NCT06633198 Heat, Microvascular Function and Aging
| NCT ID | NCT06633198 |
| Status | Recruiting |
| Phase | EARLY_Phase 1 |
| Sponsor | William Hughes |
| Condition | Aging |
| Study Type | INTERVENTIONAL |
| Enrollment | 20 participants |
| Start Date | 2025-05-01 |
| Primary Completion | 2028-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.
This trial targets 20 participants in total. It began in 2025-05-01 with a primary completion date of 2028-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Vascular dysfunction is a common factor in many chronic debilitating diseases, contributing to morbidity and mortality. With the onset of chronic disease or exposure to stress, the vasculature displays an inability to adequately respond to increased blood flow demands, manifesting in a reduced ability or altered mechanism of vasodilation. Aging is an independent risk factor in the development of cardiovascular disease, and reduces vasodilator capacity, or alters the mechanism by which vasodilation occurs in multiple vascular beds. Chronic exercise/physical activity is one of the most potent ways to enhance vascular function, resulting in favorable outcomes such as reductions in blood pressure, and improved ability to perform activities of daily living. Barriers to exercise or failure of long-term adherence preclude many populations from the cardiovascular benefits of exercise, thus further enhancing cardiovascular risk. Avenues to mimic blood flow patterns observed with exercise may exert beneficial effects without the need for the ability to exercise. Recent evidence has demonstrated that passive heat therapy, or chronic heat exposure (\~ +1°C in core temperature) results in reductions in major adverse cardiovascular events, blood pressure and improved large artery endothelial function, primarily through preservation of large artery function in response to vascular stress. It is unclear whether microvascular function is augmented in response to acute heat exposure, or whether this can protect against vascular insults particularly in older adults. Some preliminary evidence in humans suggest that autophagy, a cell recycling process is involved in the beneficial cardiovascular effects, as short-term heat exposure upregulates markers of autophagy. Previous evidence from our lab indicates that autophagy governs the mechanism by which microvascular vasodilation occurs. The role of autophagy in mediating the beneficial effects of passive heating is unknown.
Eligibility Criteria
Inclusion Criteria: * Participants must be between 18-80 yrs. of age * No more than 1 cardiovascular risk factor (see list in exclusion criteria) Exclusion Criteria: * Cardiovascular Risk Factors * Uncontrolled/unmanaged hypertension and/or use of current anti-hypertensive therapy * Current Tobacco product use or within last 6 months * BMI greater than 30 * Hyperlipidemia - diagnosed and/or taking medications to manage * Hypercholesterolemia - diagnosed and/or taking medications to manage (e.g. statins) * Type 1 or Type 2 Diabetes * Use of anti-coagulant or anti-platelet drugs * Use of beta blockers * Symptomatic coronary artery disease * Diagnosed Heart Failure (Any classification above Class I as defined by NY Heart Association) * Diagnosed renal impairment Renal impairment defined, according to National Kidney Foundation as abnormalities of kidney structure or function, present for greater than 3 months, including: * Albuminuria (ACR ≥ 30 mg/g) * Urine sediment abnormalities * Electrolyte and other abnormalities due to tubular disorders * Structural abnormalities detected by imaging * History of kidney transplantation * Decreased glomerular filtration rate (GFP \< 60 mL/min/1.73 m2) * Current Hormone Replacement Therapy Use * History of retinopathy * Documented neuromuscular disorders * Porphyria Cutanea Tarda (blistering of skin to sun; photosensitivity) * Pregnancy (Young Female subjects) * Allergies to povidone iodine * Tattoos on lower arm (forearm) * Use of erectile dysfunction medication in the past 6 months * Use of topical/non-topical steroids in last 6 months (e.g. cortisone cream) * Active anti-cancer treatment or treatment within last 12 months * Active COVID-19 or within the past 3 months * Gender Reassignment Therapy
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06633198 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Aging. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
What phase is the NCT06633198 trial and what does that mean for participants?
Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.
Is NCT06633198 currently recruiting?
Yes, NCT06633198 is actively recruiting participants. Contact the research team at whughes@mcw.edu for enrollment information.
Where is the NCT06633198 trial being conducted?
This trial is being conducted at Milwaukee, United States.
Who is sponsoring the NCT06633198 clinical trial?
NCT06633198 is sponsored by William Hughes. The trial plans to enroll 20 participants.