RecruitingNCT05442463

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

Hormone Therapy and Angiotensin-Dependent Arterial and Renal


Sponsor

University of Calgary

Enrollment

200 participants

Start Date

Nov 30, 2020

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 18 YearsMax Age: 90 Years

Inclusion Criteria2

  • Age 18 to 90 years
  • Taking hormones orally or non-orally (either estrogen, progesterone or testosterone)

Exclusion Criteria8

  • Cardiovascular disease (symptoms consistent with myocardial ischemia, previously documented myocardial ischemia, cardiac arrhythmias or valve abnormalities, or abnormal ECG at screening)
  • Cerebrovascular disease (transient ischemic attacks or stroke)
  • History of hypertension (BP>140/90 or use of antihypertensive medications)
  • Estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73m2
  • Diabetes mellitus (defined by history, use of hypoglycaemic agents or a fasting glucose >7mmol/L)
  • Current smoker
  • Previous history of preeclampsia
  • Anabolic steroids, cortical steroids, or non-steroidal anti-inflammatory medications, or at the discretion of the investigator.

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Interventions

DRUGCaptopril Tablets

Captorpril challenge to each participant

DRUGIohexol

Iohexol infusion to evaluate measured GFR


Locations(1)

University of Calgary

Calgary, Alberta, Canada

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NCT05442463