CCPA: Capsaicin for Cerebral Perfusion Augmentation

Sponsor
Instituto Mexicano del Seguro Social (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05543837
Collaborator
Centenario Hospital Miguel Hidalgo (Other)
20
1
2
4.4
4.5

Study Details

Study Description

Brief Summary

To determine the effect of capsaicin upon serial transcranial Doppler (TCD) markers of cerebral blood flow (CBF). Methods Serial TCD testing in 30 participants with cerebrovascular risk factors. Capsaicin doses .66 and .99 μMol. Outcomes: peak systolic and end-diastolic velocities in the middle cerebral artery (MCA), mean velocity (MV), pulsatility index (PI), CBF index, arterial pressure, and perceived pungency (PP) in five minutes intervals up to 20 minutes.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Subjects The study is expected to enroll 30 participants who will be recruited from the Internal Medicine outpatient clinic. Those willing to participate will be asked to sign the informed consent form (ICF) and will received the assigned dose of capsaicin. Half of the participants in each dose group will receive stimulation on either left or right side of the palate, but TCD measurements will be bilateral. Chemical stimuli From an initial 0.1% capsaicin (Sigma-Aldrich, St. Louis, MO) stock solution in 95% ethanol; solutions with 66 and 99 μMol/ml solutions will be obtained by diluting the stock solution with distilled water. One milliliter of each dilution was pipetted on to 2 cm filter paper squares. Then, the filter papers will be let dry. Immediately before application, filter papers will be rehydrated with 1 milliliter of distilled water. The rehydrated filter paper will be applied and will remain stationary on the subject's hemi palate's posterior surface during TCD measurements. Participants will be instructed not to swallow and to avoid touching the paper filter with their tongue for the 20 minutes of the experiment.

TCD testing With a TCD device (Philips Sonos 7500®) will include: peak systolic velocity (PSV) and end-diastolic velocity (EDV) in the middle cerebral artery (MCA) through the temporal window of the stimulated side. After a basal recording post stimulation recordings will initiate immediately after stimulation, and will be followed by serial recordings every five minutes and up to 20 minutes. At each time point the systolic pressure (SP), diastolic pressure (DP), and perceived pungency (PP) on a visual analog scale will be recorded. TCD markers of cerebral blood flow From the initial measurements the Mean velocity (MV) = EDV + [(PSVEDV) / 3], pulsatility index (PI) = PSV - EDV / MV, mean arterial pressure (MAP) = ((2 * DP) + SP) / 3 and, the CBF index (CBFi), CBFi = (MAP * 10) / 1.47^PI, will be calculated.

Statistical analysis Shapiro Wilkins W-Test for normality. The results of the continuous variables will be described as median (max-min) or mean+/- SD according to distribuition. The categorical variables will be described as tables of absolute and relative frequencies, and the comparisons between the groups of subjects (according to the dose of capsaicin) will be carried out with chi-square tests. To compare the variables studied between the groups of subjects (according to the different doses of capsaicin), Mann-Whitney U-Test/independent samples Student´s T-Test will be used appropriately. For comparisons of the baseline state with the changes recorded over time, various Wilcoxon signed-rank tests will be performed.The relationship between pungency ratings and MV response will be evaluated by Spearman's rho test. The level of statistical significance will be set at 0.05.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Effect of Capsaicin on the Augmentation of Cerebral Perfusion. A Phase II Study.
Anticipated Study Start Date :
Sep 20, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Feb 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Capsaicin .66μMol/ml

Group receiving .66μMol/ml

Drug: Capsaicin
Patients will receive a fixed dose of capsaicin
Other Names:
  • 8-Methyl-N-vanillyl-trans-6-nonenamide
  • Experimental: Capsaicin .99μMol/ml

    Group receiving .99μMol/ml

    Drug: Capsaicin
    Patients will receive a fixed dose of capsaicin
    Other Names:
  • 8-Methyl-N-vanillyl-trans-6-nonenamide
  • Outcome Measures

    Primary Outcome Measures

    1. Mean velocity [20 minutes]

      The Mean velocity in the Middle Cerebral Artery

    2. Pulsatility Index [20 minutes]

      A calculated flow parameter in ultrasound, derived from the maximum, minimum, and mean Doppler frequency shifts during a defined cardiac cycle.

    Secondary Outcome Measures

    1. Mean arterial pressure (MAP) [20 minutes]

      The average arterial pressure throughout one cardiac cycle, systole, and diastole.

    2. Cerebral Blood Flow index [20 minutes]

      The result of the following formula: CBFi = (MAP * 10) / 1.47^Pulsatility Index.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Signed Informed Consent Form

    • Previous diagnosis and stable condition of one of the following:

    Diabetes Mellitus Hypertension Dyslipidemia Chronic Obstructive Pulmonary Disease

    Exclusion Criteria:
    • History of alergy or hypersensibility to dietary capsaicin

    • Previous diagnosis of stroke

    • Chronic use of cholinergic/anticholinergic drugs

    • Chronic use of sympathomimetic drugs

    • Chronic use of serotonergic drugs

    • Chronic use of dopaminergic drugs

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centenario Hospital Miguel Hidalgo Aguascalientes Mexico 20259

    Sponsors and Collaborators

    • Instituto Mexicano del Seguro Social
    • Centenario Hospital Miguel Hidalgo

    Investigators

    • Principal Investigator: Juan M Marquez-Romero, MD, MSc, Unidad de Medicina de Alta Especialidad, Torre Medica CMQ

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Juan Manuel Marquez Romero, Principal Investigator, Instituto Mexicano del Seguro Social
    ClinicalTrials.gov Identifier:
    NCT05543837
    Other Study ID Numbers:
    • 2022-E-20
    First Posted:
    Sep 16, 2022
    Last Update Posted:
    Sep 16, 2022
    Last Verified:
    Sep 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Juan Manuel Marquez Romero, Principal Investigator, Instituto Mexicano del Seguro Social
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 16, 2022