Clinical trial

Human Cerebral Blood Flow Regulation: Sex, Mechanism, and Stress Differences (Phase 2)

Name
2023-0548
Description
Twenty-six otherwise healthy adults between 18-40 years of age composed of 13 males and 13 females will be enrolled in this study to determine how sex and sex hormones influence cerebral blood flow (CBF) control in healthy young adults without confounds of age or disease. Participants can expect to be on study for approximately 16 days.
Trial arms
Trial start
2023-06-13
Estimated PCD
2025-03-31
Trial end
2026-05-31
Status
Recruiting
Phase
Early phase I
Treatment
Indomethacin
to inhibit cyclooxygenase (COX)
Arms:
Indo First: Hormone Add-Back, Indo First: Hormone Suppression, Placebo First: Hormone Add-Back, Placebo First: Hormone Suppression
Other names:
Indo
Placebo
Placebo
Arms:
Indo First: Hormone Add-Back, Indo First: Hormone Suppression, Placebo First: Hormone Add-Back, Placebo First: Hormone Suppression
Orilissa
to suppress hormones 200mg dose 2x per day (all participants)
Arms:
Indo First: Hormone Add-Back, Indo First: Hormone Suppression, Placebo First: Hormone Add-Back, Placebo First: Hormone Suppression
Testosterone gel
50 mg each morning for add back phase (male participants)
Arms:
Indo First: Hormone Add-Back, Placebo First: Hormone Add-Back
Anastrozole
1mg/day in men to prevent conversion of testosterone to estradiol
Arms:
Indo First: Hormone Add-Back, Placebo First: Hormone Add-Back
Estradiol
Women will receive oral estradiol 2mg/daily
Arms:
Indo First: Hormone Add-Back, Placebo First: Hormone Add-Back, Placebo First: Hormone Suppression
Size
26
Primary endpoint
Cerebral Blow Flow (CBF): Hormone Suppression Hypoxia Condition
first set of study visits (up to 2 hours) within the first 7 days on study
Cerebral Blow Flow: Hormone Suppression Hypercapnia Condition
first set of study visits (up to 2 hours) within the first 7 days on study
Cerebral Blow Flow: Hormone Add-Back Hypoxia Condition
second set of study visits (up to 2 hours) within 12-16 days on study
Cerebral Blow Flow: Hormone Add-Back Hypercapnia Condition
second set of study visits (up to 2 hours) within 12-16 days on study
Eligibility criteria
Inclusion Criteria: * Age between ≥18 - ≤40 years inclusive * Completed Phase 1: Study 2020-0336 Exclusion Criteria: * Hypertensive * \> 125 mmHg systolic blood pressure; or * \> 80 mmHg diastolic blood pressure * BMI ≥25 kg/m2 * Fasting blood glucose ≥100 mg/dl * LDL cholesterol ≥130 mg/dl * Triglycerides ≥150 mg/dl * Current diagnosis or history of: * peripheral vascular disease * hepatic disease * renal disease * lung disease * gastrointestinal disorders/bleeding * hematologic disease * stroke * myocardial infarction * coronary heart disease * congestive heart failure * heart surgery * prediabetes * diabetes mellitus (type 1, type 2, MODY, or others) * sleep apnea * hypertension * some autoimmune diseases, such as inflammatory bowel disease or systemic lupus erythematosus (exclusion at discretion of reviewing MD) * Current smoking, defined as the use of tobacco or nicotine products \>5 times in the past 30 days. * Cardiovascular medication use * NSAID sensitivity * Magnesium-restricted diet * Any contraindications of having an MRI * (e.g. the requirement of anxiolytics in order to complete an MRI scan) * Irregular menstrual cycle (females only) * Medical conditions that can affect the menstrual cycle, such as hyperprolactinemia, prolactinoma, hypercortisolemia, and congenital adrenal hyperplasia (females only) * Pregnancy, breast feeding, or plans to conceive within the next 3 months (females only) * Polycystic ovary syndrome (females only) * Hirsutism defined as unwanted and/or excessive hair growth on the face, chest, or back (females only) * Levonorgestrel intrauterine device (IUD) (females only) * Hormonal birth control will not be allowed in women, in order to control for high variability between type, dose, and route of therapy. However, in discussion with Dr. Davis (Co-I) and Dr. Laura Cooney M.D., physician experts in medical and reproductive endocrinology and infertility, there are two broad exceptions to this birth control criteria: * Copper intrauterine devices (IUDs) will be allowed as they do not change systemic sex hormone levels). * Women currently taking hormonal birth control (i.e. contraceptive pills, patch, ring) for contraception only (not for a medical condition such as those listed in exclusion criteria above) may consider temporarily stopping to become eligible for enrollment. Hormonal birth control must be stopped at least one month prior to Study Visit 1 to provide time for menstruation to resume. Then stoppage continues through the last planned study visit. Screening information will be reviewed by endocrinology physicians to determine eligibility and timing on this issue.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'FACTORIAL', 'interventionModelDescription': 'double-blind placebo controlled design', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 26, 'type': 'ESTIMATED'}}
Updated at
2024-04-23

1 organization

6 products

1 indication

Product
Placebo
Product
Orilissa
Product
Estradiol