Study of Nasal Insulin to Fight Forgetfulness - Long-acting Insulin Detemir - 120 Days (SL120)

• Sponsor: Wake Forest University Health Sciences (Other)
• Overall Status: Completed
• CT.gov ID: NCT01595646
• Collaborator: Alzheimer's Association (Other)
• Enrollment: 37
• Locations: 2
• Arms: 3
• Actual Duration (Months): 40.3
• Patients Per Site: 18.5
• Patients Per Site Per Month: 0.5

Study Details

Study Description

Brief Summary

The study will examine the effects of intranasally administered long-acting insulin detemir on cognition in persons with Alzheimer's disease (AD) or amnestic mild cognitive impairment (aMCI). The rationale for these studies is derived from growing evidence that insulin contributes to multiple brain functions, and that insulin dysregulation can contribute to AD pathogenesis. Thus, therapies aimed at restoring normal insulin signaling in the CNS may have beneficial effects on brain function. Intranasal administration of insulin increases insulin signaling in the brain without raising peripheral levels and causing hypoglycemia. Insulin detemir is an insulin analogue that may have better action in brain than other insulin formulations because of its albumin binding properties. The investigators will test the therapeutic effects of intranasally-administered insulin detemir in a study in which participants will receive insulin detemir, regular insulin, or placebo over a four month period. The investigators will test the hypothesis that insulin and insulin detemir will both improve memory and daily functioning in persons with AD/aMCI compared with placebo, but that insulin detemir will have the greatest effect.

Condition or Disease	Intervention/Treatment	Phase
Alzheimer's Disease; Mild Cognitive Impairment	Drug: Saline; Drug: Insulin detemir; Drug: Insulin	Phase 2

Detailed Description

It is well-known that insulin, a hormone that is naturally secreted by the pancreas, plays an important physiological role by regulating blood sugar levels in the body. Researchers now know that insulin plays many important roles in the brain as well. Insulin seems to be especially active in the part of the brain that corresponds to learning and memory. Studies have shown that when people have insufficient insulin in the brain (which, for example, is the case with Type-II diabetes), they are increasingly at risk to develop memory problems and Alzheimer's disease. In a past study, the investigators administered intravenous insulin to participants and found that it improves memory. However, that particular method would not be a practical intervention for people with Alzheimer's disease due to the risks of hypoglycemia or exacerbation of insulin resistance. Instead, the investigators use an "intranasal" method of administration, in which the insulin is inserted into a device, and administered intranasally. In this method, the insulin travels directly to the brain, and bypasses the body. Past studies have also demonstrated that this can be a reliable way to improve memory, and it does not change the body's blood glucose levels.

In our past studies, investigators have used regular insulin, which lasts about 3-4 hours and creates a similar "spike" in insulin that one would have after eating a meal. However, in normal physiology, the pancreas also releases small and more constant "pulses" of insulin throughout the day and night, establishing a base level of insulin. Accordingly, several longer-lasting types of insulin are now available that last closer to 10-12 hours, mimicking that basal level of insulin. The current study uses a long-lasting type of insulin called "insulin detemir," to determine if learning and memory will benefit from a more consistent supplement of insulin. The investigators want to determine whether this treatment can benefit people who already have a memory impairment-either they have a diagnosis of Alzheimer's disease (AD) or have a mild cognitive impairment (MCI), a condition that precedes Alzheimer's disease. The investigators will examine cognition, daily function, cerebral blood flow, and different markers of Alzheimer's disease that are in the blood and cerebral spinal fluid (CSF) as outcome measures.

The investigators have these specific aims:

1. We will test the hypothesis that compared to placebo, four months of treatment with intranasal insulin or insulin detemir will improve cognition and function in adults with AD or MCI, but that greater effects will be observed for insulin detemir.

2. We will examine the effects of intranasal insulin and insulin detemir on cerebral blood flow in adults with AD or MCI.

3. We will examine the effects of intranasal insulin and insulin detemir on CSF Aβ, tau and inflammatory markers in adults with AD or MCI.

To examine these hypotheses, the investigators are recruiting approximately 90 participants who have been diagnosed with AD or mild cognitive impairment. They will be randomly selected to take a placebo (saline), insulin detemir, or insulin. Cognition, the level of daily functioning, glucose tolerance, and cerebral blood flow will be tested before they begin the study drug, and after 16 weeks of the study drug. Some participants will also undergo a lumbar puncture both before beginning study drug and after 16 weeks of taking the study drug.

Statistical analysis will follow an intent-to-treat (ITT) approach; that is, subjects will be analyzed in their original randomized group regardless of adherence to group assignment. A completer analysis will also be performed, including only those subjects who successfully complete the treatment phase. Missing data will be handled using multiple imputation linear regression. We will conduct secondary analyses on other measures of cognition, daily function, cerebral blood flow, and CSF biomarkers. For ASL-MRI, following coregistration and processing, parametric maps will be generated to determine regional CBF values by treatment group. Secondary analyses will also examine treatment duration (2-month vs. 4-month) for all relevant outcomes. All models will be adjusted for age and an index of peripheral insulin sensitivity (derived from 120-minute OGTT glucose and insulin values) if statistically warranted, and posthoc contrasts will be performed when appropriate. Secondary analyses will also evaluate whether treatment response of cognition, daily function, CSF and plasma markers, and insulin differ according to APOE4 genotype. Although these analyses will be exploratory due to possible limited APOE4 by treatment arm cell size, the data will be examined for statistical trends that warrant further exploration in larger trials. Other secondary analyses will examine associations among treatment-related outcomes using scores derived from multiple regression of data collected during the treatment phase residualized with respect to baseline values.

Study Design

• Study Type: Interventional
• Actual Enrollment: 37 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: Study of Nasal Insulin to Fight Forgetfulness - Long-acting Insulin Detemir - 120 Days (SL120)
• Actual Study Start Date: Nov 1, 2011
• Actual Primary Completion Date: Mar 12, 2015
• Actual Study Completion Date: Mar 12, 2015

Arms and Interventions

Arm	Intervention/Treatment
Placebo Comparator: Saline Saline placebo taken twice per day via intranasal route.	Drug: Saline; Saline, administered intranasally twice per day for a 16 week duration; Other Names: Saline solution
Experimental: Insulin Detemir 20IU of Insulin Detemir taken twice per day (40IU total per day) via intranasal route	Drug: Insulin detemir; 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day); Other Names: Levemir
Experimental: Insulin 20IU Insulin, administered twice per day (40IU total per day) via intranasal route	Drug: Insulin; 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day); Other Names: Novolin R

Outcome Measures

Primary Outcome Measures

1. Verbal Memory Composite [Change from Baseline in Verbal Memory at 16 weeks]

   The composite will consist of the sum of Z scores for Delayed Story Recall and Buschke Selective Reminding Test. In the Story Recall test subjects listen to a story containing 44 informational bits that is read once. Subjects will be asked to recall the story immediately after the reading and after a 20-min delay. Credit is awarded for each bit recalled verbatim or accurately paraphrased. The Buschke Selective Reminding Test measures verbal memory through multiple trials of a list learning task. A list of 12 words is audibly presented to the subject, and subjects recall as many words as possible. On subsequent trials, subjects are only told those words they omitted on the previous trial. The procedure continues until the subject recalls all words on two successive trials or to the twelfth trial. After a 30-minute delay, subjects recall as many items as possible. Number of items recalled after the delay will be summed. Higher scores indicate better performance.

Secondary Outcome Measures

1. Cerebral Spinal Fluid (CSF) Biomarkers of AD [Change from Baseline in CSF Biomarkers at 16 Weeks]

   CSF Abeta (Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject.

2. Cerebral Spinal Fluid (CSF) Biomarkers of AD TTau-P181/Abeta42 Ratio [Change from Baseline in CSF Biomarkers at 16 Weeks]

   CSF Abeta (ABeta 38, ABeta 40, and Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject. A pre and post ratio of TTau-P181/Abeta42 will be given.

3. Functional Ability [baseline, month 2, and month 4]

   Subjects will have a collateral informant (i.e., spouse or friend) rate the subjects' ability to carry out activities of daily living on the Dementia Severity Rating Scale. The Dementia Severity Rating Scale is made up of sub-scales and the scores from each are summed to produce one score. The scale assess memory, ability to get from place to place, and speech and language each with a range from 0-6; recognition of family members and social and community both having a range from 0-5; orientation of time, orientation to place, ability to make decisions, home activities and responsibilities, and control of urination and bowels each having a range of 0-4; personal care- cleanliness and eating both with a range of 0-3. The total score range is from 0-54 and lower scores denotes better outcomes.

4. The Alzheimer's Disease Assessment Scale-Cognitive [ADAS-Cog/Alzheimer's Disease Cooperative Study (ADCS)] - MCI Revision [Baseline, Month 2 and Month 4]

   This cognitive screening measure contains measures of confrontational naming, following commands, constructional praxis, ideational praxis, orientation, and language production and comprehension. Total scores range from 0-70, with higher scores indicating greater cognitive impairment.

Other Outcome Measures

1. Executive Function Composite [Change from Baseline in Executive Functioning at 16 Weeks]

   Sum of Z Scores from Dot Counting Test (test of executive functioning) and Benton Visual Retention Test Form F&G (a test of visual working memory)

2. Plasma Biomarkers of AD [Change from Baseline in Plasma Biomarkers at 16 Weeks]

   Plasma Abeta (ABeta 38, ABeta 40, and Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject.

3. Cerebral Blood Flow [Change from Baseline in Cerebral Blood Flow at 16 Weeks]

   Functional MRI and arterial-spin labeling perfusion MRI

4. Glucose Tolerance [Change from Baseline in Glucose Tolerance at 16 Weeks]

   Subjects will undergo oral glucose tolerance test (OGTT) to assess glucose tolerance

Eligibility Criteria

Criteria

• Ages Eligible for Study: 50 Years to 89 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Age 50-89

• Diagnosed with mild cognitive impairment, or mild/moderate AD

Exclusion Criteria:

• Excessively high or low blood pressure, heart rate

• Pre-existing diabetes not controlled by exercise/diet

• Previous/current use of insulin

• Significant elevations in lipids, liver enzymes

• Menstrual period within the last 12 months

• Significant neurological or medical disorder (other than AD)

• Significant use of nasal decongestants

• Current use of anti-psychotic, anti-convulsive, anxiolytic, glucocorticoids, or sedative medications

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Wake Forest Baptist Hospital	Winston-Salem	North Carolina	United States	27157
2	VA Puget Sound Health Care System - American Lake Division	Tacoma	Washington	United States	98493

Sponsors and Collaborators

• Wake Forest University Health Sciences
• Alzheimer's Association

Investigators

• Principal Investigator: Suzanne Craft, PhD, Wake Forest University Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Wake Forest University Health Sciences
• ClinicalTrials.gov Identifier: NCT01595646
• Other Study ID Numbers: IRB00023230; ZEN-10-173646US
• First Posted: May 10, 2012
• Last Update Posted: Nov 17, 2020
• Last Verified: Apr 1, 2018

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Wake Forest University Health Sciences: Memory; Intranasal insulin; Alzheimer's disease; Mild Cognitive Impairment
• Additional relevant MeSH terms: Alzheimer Disease; Cognitive Dysfunction; Insulin; Insulin, Globin Zinc; Insulin Detemir

Study Results

Participant Flow

Arm/Group Title	Saline	Insulin Detemir	Insulin
Arm/Group Description	Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
Period Title: Overall Study
STARTED	13	12	12
COMPLETED	12	12	12
NOT COMPLETED	1	0	0

Baseline Characteristics

Arm/Group Title	Saline	Insulin Detemir	Insulin	Total
Arm/Group Description	Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)	Total of all reporting groups
Overall Participants	12	12	12	36
Age (Count of Participants)
<=18 years	0 0%	0 0%	0 0%	0 0%
Between 18 and 65 years	4 33.3%	4 33.3%	3 25%	11 30.6%
>=65 years	8 66.7%	8 66.7%	9 75%	25 69.4%
Age (years) [Mean (Full Range) ]
Mean (Full Range) [years]	68	66	68	68
Sex: Female, Male (Count of Participants)
Female	6 50%	6 50%	7 58.3%	19 52.8%
Male	6 50%	6 50%	5 41.7%	17 47.2%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native	0 0%	0 0%	0 0%	0 0%
Asian	0 0%	0 0%	0 0%	0 0%
Native Hawaiian or Other Pacific Islander	0 0%	0 0%	0 0%	0 0%
Black or African American	0 0%	0 0%	0 0%	0 0%
White	12 100%	12 100%	12 100%	36 100%
More than one race	0 0%	0 0%	0 0%	0 0%
Unknown or Not Reported	0 0%	0 0%	0 0%	0 0%

Outcome Measures

1. Primary Outcome

Title	Verbal Memory Composite
Description	The composite will consist of the sum of Z scores for Delayed Story Recall and Buschke Selective Reminding Test. In the Story Recall test subjects listen to a story containing 44 informational bits that is read once. Subjects will be asked to recall the story immediately after the reading and after a 20-min delay. Credit is awarded for each bit recalled verbatim or accurately paraphrased. The Buschke Selective Reminding Test measures verbal memory through multiple trials of a list learning task. A list of 12 words is audibly presented to the subject, and subjects recall as many words as possible. On subsequent trials, subjects are only told those words they omitted on the previous trial. The procedure continues until the subject recalls all words on two successive trials or to the twelfth trial. After a 30-minute delay, subjects recall as many items as possible. Number of items recalled after the delay will be summed. Higher scores indicate better performance.
Time Frame	Change from Baseline in Verbal Memory at 16 weeks

Outcome Measure Data

Analysis Population Description

The study is in data analysis and manuscript write-up.

Arm/Group Title	Saline	Insulin Detemir	Insulin
Arm/Group Description	Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
Measure Participants	12	12	12
Mean (Standard Error) [Change in Z score memory composite]	-.31247583 (.23)	.33390008 (.23)	-.05181561 (.22)

2. Secondary Outcome

Title	Cerebral Spinal Fluid (CSF) Biomarkers of AD
Description	CSF Abeta (Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject.
Time Frame	Change from Baseline in CSF Biomarkers at 16 Weeks

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Saline	Insulin Detemir	Insulin
Arm/Group Description	Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
Measure Participants	12	12	12
Abeta42 Pre	331.5 (148.4)	408.5 (196.9)	305.5 (86.1)
Abeta 42 Post	384 (212)	381.8 (227.8)	325 (92.1)
Tau Pre	109.7 (27)	118.3 (49.1)	132.3 (71)
Tau Post	117.1 (36.8)	107.6 (56)	152.2 (106.7)
Tau-P181 Pre	65.1 (33.1)	63.9 (28)	74 (28.9)
Tau-P181 Post	72.17 (25.3)	64.1 (19.8)	68.5 (39.7)

3. Secondary Outcome

Title	Cerebral Spinal Fluid (CSF) Biomarkers of AD TTau-P181/Abeta42 Ratio
Description	CSF Abeta (ABeta 38, ABeta 40, and Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject. A pre and post ratio of TTau-P181/Abeta42 will be given.
Time Frame	Change from Baseline in CSF Biomarkers at 16 Weeks

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Saline	Insulin Detemir	Insulin
Arm/Group Description	Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
Measure Participants	12	12	12
TTau-P181/Abeta42 ratio Pre	.27 (19)	.23 (.22)	.27 (.14)
Tau-P181/Abeta42 ratio Post	.30 (.21)	.23 (.16)	.23 (.13)

4. Secondary Outcome

Title	Functional Ability
Description	Subjects will have a collateral informant (i.e., spouse or friend) rate the subjects' ability to carry out activities of daily living on the Dementia Severity Rating Scale. The Dementia Severity Rating Scale is made up of sub-scales and the scores from each are summed to produce one score. The scale assess memory, ability to get from place to place, and speech and language each with a range from 0-6; recognition of family members and social and community both having a range from 0-5; orientation of time, orientation to place, ability to make decisions, home activities and responsibilities, and control of urination and bowels each having a range of 0-4; personal care- cleanliness and eating both with a range of 0-3. The total score range is from 0-54 and lower scores denotes better outcomes.
Time Frame	baseline, month 2, and month 4

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Saline	Insulin Detemir	Insulin
Arm/Group Description	Saline placebo taken twice per day via intranasal route. Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) via intranasal route Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) via intranasal route Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
Measure Participants	12	12	12
Baseline	7.3 (6.9)	8.7 (6.7)	7.7 (6.8)
month 2	7 (6.7)	9.7 (7.3)	9.7 (7.4)
month 4	6.9 (7.1)	9.1 (7.5)	10.6 (9.4)

5. Secondary Outcome

Title	The Alzheimer's Disease Assessment Scale-Cognitive [ADAS-Cog/Alzheimer's Disease Cooperative Study (ADCS)] - MCI Revision
Description	This cognitive screening measure contains measures of confrontational naming, following commands, constructional praxis, ideational praxis, orientation, and language production and comprehension. Total scores range from 0-70, with higher scores indicating greater cognitive impairment.
Time Frame	Baseline, Month 2 and Month 4

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Saline	Insulin Detemir	Insulin
Arm/Group Description	Saline placebo taken twice per day via intranasal route. Saline: Saline, administered intranasally twice per day for a 16 week duration	20IU of Insulin Detemir taken twice per day (40IU total per day) via intranasal route Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)	20IU Insulin, administered twice per day (40IU total per day) via intranasal route Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
Measure Participants	12	12	12
Baseline	20 (11.7)	21.6 (13.7)	19.8 (12.8)
Month 2	18.5 (11.8)	23.4 (17.1)	21.8 (13.6)
Month 4	20.4 (13.7)	19.5 (12.9)	22.6 (15.8)

6. Other Pre-specified Outcome

Title	Executive Function Composite
Description	Sum of Z Scores from Dot Counting Test (test of executive functioning) and Benton Visual Retention Test Form F&G (a test of visual working memory)
Time Frame	Change from Baseline in Executive Functioning at 16 Weeks

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title

Arm/Group Description

7. Other Pre-specified Outcome

Title	Plasma Biomarkers of AD
Description	Plasma Abeta (ABeta 38, ABeta 40, and Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject.
Time Frame	Change from Baseline in Plasma Biomarkers at 16 Weeks

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title

Arm/Group Description

8. Other Pre-specified Outcome

Title	Cerebral Blood Flow
Description	Functional MRI and arterial-spin labeling perfusion MRI
Time Frame	Change from Baseline in Cerebral Blood Flow at 16 Weeks

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title

Arm/Group Description

9. Other Pre-specified Outcome

Title	Glucose Tolerance
Description	Subjects will undergo oral glucose tolerance test (OGTT) to assess glucose tolerance
Time Frame	Change from Baseline in Glucose Tolerance at 16 Weeks

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title

Arm/Group Description

Adverse Events

Arm/Group Title	Saline		Insulin Detemir		Insulin
Arm/Group Description	Saline: Saline, administered intranasally twice per day for a 16 week duration		20IU of Insulin Detemir taken twice per day (40IU total per day) Insulin detemir: 20IU of insulin detemir, administered intranasally twice per day for a 16 week duration (total of 40IU insulin detemir per day)		20IU Insulin, administered twice per day (40IU total per day) Insulin: 20IU insulin, administered intranasally twice per day for a 16 week duration (total of 40IU insulin per day)
All Cause Mortality
	Saline		Insulin Detemir		Insulin
	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events
Total	0/12 (0%)		0/12 (0%)		0/12 (0%)
Serious Adverse Events
	Saline		Insulin Detemir		Insulin
	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events
Total	0/12 (0%)		0/12 (0%)		0/12 (0%)
Other (Not Including Serious) Adverse Events
	Saline		Insulin Detemir		Insulin
	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events	Affected / at Risk (%)	# Events
Total	4/12 (33.3%)		0/12 (0%)		0/12 (0%)
Cardiac disorders
Chest pain	1/12 (8.3%)	1	0/12 (0%)	0	0/12 (0%)	0
General disorders
Congestion	1/12 (8.3%)	1	0/12 (0%)	0	0/12 (0%)	0
Cold & Flu Symptoms	1/12 (8.3%)	1	0/12 (0%)	0	0/12 (0%)	0
Nervous system disorders
Anxiety	1/12 (8.3%)	1	0/12 (0%)	0	0/12 (0%)	0

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.