Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05442463

Hormone Therapy and Angiotensin-Dependent Arterial and Renal Vasoconstriction in Humans

Hormone Therapy and Angiotensin-Dependent Arterial and Renal

Status
Recruiting
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
University of Calgary · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Accepted

Summary

1. to investigate the association between route of administration of exogenous estrogen (transdermal vs. oral) and cardiorenal risk in cisgender (gender identity aligning with sex at birth) and transgender (gender identity not aligning with sex at birth) women. 2. to investigate the association between exogenous testosterone exposure and cardiorenal risk in cisgender (gender identity aligning with sex at birth) and transgender (gender identity not aligning with sex at birth) men.

Detailed description

Participants are screened for eligibility. Study involves a 4.5 hour morning in the lab: 1. Participants come fasting 2. IV infusion and blood draws 3. Non invasive testing - Holter monitor, sphygmocor, bioelectrical impedance, blood pressure checks

Conditions

Interventions

TypeNameDescription
DRUGCaptopril TabletsCaptorpril challenge to each participant
DRUGIohexolIohexol infusion to evaluate measured GFR

Timeline

Start date
2020-11-30
Primary completion
2025-11-30
Completion
2025-11-30
First posted
2022-07-05
Last updated
2025-03-27

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05442463. Inclusion in this directory is not an endorsement.