Cardiovascular Diseases Clinical Trial
Official title:
Sex-specific Effects of Continuous Estrogen on Human in Vivo Microvascular Function
NCT number | NCT06043310 |
Other study ID # | PRO40920 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | June 2, 2023 |
Est. completion date | December 2029 |
The goal of this study is to learn how long-term use of estrogen affects blood vessels in healthy adults who were assigned male at birth. Participants will: - give one blood draw of 5 mL - have a camera placed under the tongue to take pictures of blood vessels - have 2 laser Doppler microdialysis catheters placed on the forearm to monitor blood vessels before and after local drug infusion Researchers will compare blood vessel function of those who take estrogen supplements to those who do not.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | December 2029 |
Est. primary completion date | December 2029 |
Accepts healthy volunteers | |
Gender | Male |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Adults aged 18-60 years - Identify as assigned male at birth (AMAB) +/- continuous estrogen treatment for a minimum of 1 year. - Blood pressure <140/ < 90 mmHg - No more than 1 cardiovascular risk factor Exclusion Criteria: - BMI >35 - Medications that could alter cardiovascular control - Rash, skin disease, or pigmentation disorders - Anemia - Kidney Disease - Known skin allergies - Smoking or tobacco use within last 6 months - Coronary Artery Disease - > 1 cardiovascular risk factor - Hypertension - Diabetes - Hypercholesterolemia - Hyperlipidemia - Bleeding disorders - Use of anti-coagulants - Allergies to study drugs - Erectile dysfunction medication in the past 6 months - Use of topical/non-topical steroids in last 6 months - Internal mouth sores |
Country | Name | City | State |
---|---|---|---|
United States | Froedtert Hospital | Wauwatosa | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Medical College of Wisconsin |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in blood vessel dilation | Cutaneous vascular conductance in response to acetylcholine, L-NAME, and sodium nitroprusside infusions will be calculated as percentage of cardiovascular conductance. | 2 hours | |
Primary | Change in Perfused Vessel Density | Total vessel density (TVD) will be calculated using the DeBacker Score manual analysis on all images that have a minimum microcirculation image quality score (MIQS) of 10. Perfused vessel density (PVD) will be calculated by multiplying total vessel density (TVD) x proportion of perfused vessels (PPV%). | 0.5 hours |
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