CompletedPhase 4NCT03834883
Reducing the Risk of Drug-Induced QT Interval Lengthening in Women
Studying Congenital long QT syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Indiana University
- Principal Investigator
- James E Tisdale, PharmDPurdue University
- Intervention
- Progesterone(drug)
- Enrollment
- 27 enrolled
- Eligibility
- 21 years · FEMALE
- Timeline
- 2019 – 2024
Study locations (1)
- Indiana University, Indianapolis, Indiana, United States
Collaborators
American Heart Association · Purdue University
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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