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Search / Trial NCT03078829

The Relation of GnRH Treatment to QTc Interval in Transgender Females

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Mar 7, 2017

Trial Information

Current as of May 19, 2025

Terminated

Keywords

Gender Identity Trans Female Gn Rh Agonists Q Tc Interval

ClinConnect Summary

This study is a quasi-experimental time series study, designed to examine the relation between GnRH agonist treatment for 6 months in transgender female youth and electrocardiographic change in QTc interval. Study subjects will be identified when visiting the UCSF Child and Adolescent Gender Center (CAGC). A baseline electrocardiogram (ECG) will be obtained in clinic before initiation of GnRH agonist treatment and at the 6 months follow up appointment.

Sampling scheme: Consecutive sample of transfemale patients presenting to UCSF CAGC (Child and Adolescent Gender Center) clinics meeting en...

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • 1. Transgender males to females in pubertal stage Tanner stage 4-5
  • 2. starting GnRH agonist treatment
  • Exclusion Criteria:
  • 1. Heart disease or arrhythmias at base line
  • 2. Electrolyte abnormalities at baseline (abnormal serum levels of calcium, potassium or magnesium)
  • 3. Failure to obtain informed consent from a parent or guarding or informed assent from a youth.

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

San Francisco, California, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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