Probiotic Supplementation Among Adults With Recurrent Gastrointestinal Symptoms

• Sponsor: University of Maryland, Baltimore (Other)
• Overall Status: Completed
• CT.gov ID: NCT02277431
• Collaborator: (none)
• Enrollment: 80
• Arms: 2
• Duration (Months): 10

Study Details

Study Description

Brief Summary

Participants experiencing recurrent gastrointestinal symptoms in this double-blind, randomized, controlled trial will receive either a commercially-available probiotic dietary supplement or placebo. The investigators hypothesize that participants in the probiotic dietary supplement group will experience greater improvement in their gastrointestinal symptoms than participants in the placebo group.

Condition or Disease	Intervention/Treatment	Phase
Gastrointestinal Symptoms; Bloating; Gas; Indigestion; Abdominal Pain; Defecation Irregularity	Dietary Supplement: Probiotic dietary supplement (Trenev Trio®); Dietary Supplement: placebo	Phase 2/Phase 3

Study Design

• Study Type: Interventional
• Actual Enrollment: 80 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Double (Participant, Investigator)
• Primary Purpose: Other
• Official Title: A Randomized Controlled Trial of a Commercially-Available Probiotic Supplement (Trenev Trio®/Healthy Trinity®) and the Promotion of Normal Gastrointestinal Function Among Adults With Recurrent Gastrointestinal Symptoms
• Study Start Date: Dec 1, 2014
• Actual Primary Completion Date: Sep 1, 2015
• Actual Study Completion Date: Oct 1, 2015

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Probiotic dietary supplement Trenev Trio® (healthcare professional line)/Healthy Trinity® (consumer line) is a dietary supplement that contains probiotics microenrobed in an oil matrix in a two-piece hard gel capsule. One capsule will be taken twice per day (am & pm) offering a total daily serving of: Lactobacillus acidophilus NAS super strain (10 billion Colony Forming Units [CFU]) Bifidobacterium bifidum Malyoth super strain (40 billion CFU) Lactobacillus delbrueckii subspecies bulgaricus LB-51 super strain (10 billion CFU)	Dietary Supplement: Probiotic dietary supplement (Trenev Trio®); Trenev Trio® (healthcare professional line)/Healthy Trinity® (consumer line) is a dietary supplement that contains probiotics microenrobed in an oil matrix in a two-piece hard gel capsule. One capsule will be taken twice per day (am & pm) offering a total daily serving of: Lactobacillus acidophilus NAS super strain (10 billion Colony Forming Units [CFU]) Bifidobacterium bifidum Malyoth super strain (40 billion CFU) Lactobacillus delbrueckii subspecies bulgaricus LB-51 super strain (10 billion CFU)
Placebo Comparator: Placebo The placebo capsules utilized in this study will be indistinguishable from the probiotic dietary supplement capsules as they will be identical in appearance, odor, weight, and taste. Furthermore, the same sunflower oil matrix will be in both the probiotic dietary supplement and placebo. The only difference between the dietary supplement and placebo capsules will be the probiotic bacteria.	Dietary Supplement: placebo

Outcome Measures

Primary Outcome Measures

1. Severity of self-reported bloating [Study end (6 weeks from baseline)]

   Likert scale

2. Severity of self-reported gas [Study end (6 weeks from baseline)]

   Likert scale

3. Severity of self-reported indigestion [Study end (6 weeks from baseline)]

   Likert scale

4. Severity of self-reported abdominal pain [Study end (6 weeks from baseline)]

   Likert scale

5. Severity of self-reported defecation irregularity [Study end (6 weeks from baseline)]

   Likert scale

Secondary Outcome Measures

1. Frequency of self-reported bloating [Study end (6 weeks from baseline)]

   Likert scale

2. Frequency of self-reported gas [Study end (6 weeks from baseline)]

   Likert scale

3. Frequency of self-reported indigestion [Study end (6 weeks from baseline)]

   Likert scale

4. Frequency of self-reported abdominal pain [Study end (6 weeks from baseline)]

   Likert scale

5. Frequency of self-reported defecation irregularity [Study end (6 weeks from baseline)]

   Likert scale

Other Outcome Measures

1. Gastrointestinal Symptom Rating Scale [Study end (6 weeks from baseline)]

2. Gastrointestinal Quality of Life Index [Study end (6 weeks from baseline)]

3. Bristol Stool Scale [Study end (6 weeks from baseline)]

4. Rescue medication usage [Study end (6 weeks from baseline)]

5. Adequate relief [Study end (6 weeks from baseline)]

   "In the past 7 days, have you had adequate relief of your gastrointestinal discomfort?"

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

1. Self-reported response of "moderate discomfort" or worse (3 or greater on 1-5 Likert Scale) and "frequent discomfort" or more often (3 or greater on 1-5 Likert scale) from at least 2 of the following gastrointestinal symptoms: gas, indigestion, bloating, abdominal pain, or defecation irregularity as expressed on Likert scale (1=very minor or no discomfort, 2=minor discomfort, 3=moderate discomfort, 4=high discomfort, 5=very high discomfort) over the previous 3 weeks

2. Agree to continue with typical diet and exercise habits during study

3. Agree to use contraception or abstinence throughout study period, unless postmenopausal or surgically sterile (females only)

4. Able to understand and voluntarily consent to the study and understand its nature and purpose including potential risks and side effects

Exclusion Criteria:

1. Current and documented diagnosis of Inflammatory Bowel Disease (Crohn's disease or ulcerative colitis), Celiac disease, active peptic ulcer, active diverticulitis, and other active cases of gastrointestinal diseases that, in the investigators' opinions, may affect participant safety.

2. Current and documented diagnosis of any other non-gastrointestinal disease that, in the investigators' opinions, may affect participant safety or confound the evaluation of the study outcomes. Excluded conditions include congestive heart failure, malignancy, uncontrolled diabetes mellitus, uncontrolled autoimmune disease (lupus, rheumatoid arthritis, eczema), eating disorders, and any other active health condition or disease that the investigators feel contradict the intended study population of participants in good health.

3. Daily consumption of another probiotic supplement or new consumption of fermented dairy products (yogurt, kefir, etc.)

4. Usage of systemic steroids during the past 2 months

5. Usage of antipsychotic medications during the past 2 months

6. Usage of prednisone, 6-mercaptopurine, adalimumab, etanercept, infliximab, leflunomide, golimumab, or mycophenolate mofetil during the past 2 months

7. Uncontrolled anxiety or current medication for anxiety disorder

8. Pregnant or breastfeeding females

9. History of alcohol, drug, or medication abuse

10. Known allergies to any substance in the study product

11. Previous major gastrointestinal tract surgery (colon resection, gastric bypass, etc.)

12. Participation in another clinical trial within 30 days of screening

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• University of Maryland, Baltimore

Investigators

• Principal Investigator: Chris D'Adamo, PhD, University of Maryland, College Park

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Chris D'Adamo, Assistant Professor Department of Family and Community Medicine Department of Epidemiology and Public Health Director of Research Center for Integrative Medicine, University of Maryland, Baltimore
• ClinicalTrials.gov Identifier: NCT02277431
• Other Study ID Numbers: 00007145
• First Posted: Oct 29, 2014
• Last Update Posted: Sep 14, 2021
• Last Verified: Sep 1, 2021

• Additional relevant MeSH terms: Abdominal Pain; Dyspepsia

Study Results

No Results Posted as of Sep 14, 2021