CompletedPhase 4NCT03834883

Reducing the Risk of Drug-Induced QT Interval Lengthening in Women

Studying Congenital long QT syndrome

Last synced from ClinicalTrials.gov

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
Indiana University
Principal Investigator
James E Tisdale, PharmD
Purdue University
Intervention
Progesterone(drug)
Enrollment
27 enrolled
Eligibility
21 years · FEMALE
Timeline
20192024

Study locations (1)

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.

Open NCT03834883 on ClinicalTrials.gov

Other trials for Congenital long QT syndrome

Additional recruiting or active studies for the same condition.

See all trials for Congenital long QT syndrome

← Back to all trials