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Trials / Completed

CompletedNCT02513940

Influence of Testosterone Administration on Drug-Induced QT Interval Prolongation and Torsades de Pointes

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Indiana University · Academic / Other
Sex
Male
Age
65 Years
Healthy volunteers
Accepted

Summary

Torsades de pointes (TdP) is a potentially fatal ventricular arrhythmia associated with corrected QT (QTc) interval prolongation. More than 50 commonly used drugs available on the US market may cause QTc interval prolongation and TdP. While TdP occurs more commonly in women, 33-45% of all cases of TdP have occurred in men. Older age is a risk factor for drug-induced TdP in men, possibly due to declining serum testosterone concentrations. Available evidence shows an inverse relationship between QTc intervals and serum testosterone concentrations. In addition, experimental data, including those from the investigators' laboratory, suggest that both exogenous testosterone or progesterone administration may be protective against prolongation of ventricular repolarization and TdP. Specific Aim: Establish the influence of transdermal testosterone administration and oral progesterone administration as preventive methods by which to diminish the degree of drug-induced QT interval prolongation in men 65 years of age or older. Hypothesis: Transdermal testosterone administration and oral progesterone administration both effectively attenuate drug-induced QT interval response in older men. To test this hypothesis, transdermal testosterone, oral progesterone or placebo will be administered in a 3-way crossover study to men 65 years of age or older. QTc interval response to low-dose ibutilide will be assessed. The primary endpoints will be Fridericia-corrected QT interval (QTF) response to ibutilide, in the presence and absence of testosterone, and in the presence or absence of progesterone: 1) Effect on pre-ibutilide QTF, 2) Effect on maximum post-ibutilide QTF, 3) Effect on % change in post-ibutilide QTF, and 2) Area under the QTF interval-time curves.

Conditions

Interventions

TypeNameDescription
DRUGTestosteroneSubjects will receive transdermal testosterone gel 1% 100 mg daily for 7 days
DRUGProgesteroneSubjects will receive oral progesterone 400 mg (two x 200 mg capsules) once daily every evening for 7 days
DRUGPlaceboSubjects will receive placebo transdermal gel and placebo (lactose) capsules
DRUGIbutilideIbutilide 0.003 mg/kg administered to all subjects in all phases to moderately lengthen the QT interval

Timeline

Start date
2016-05-01
Primary completion
2017-10-19
Completion
2017-10-19
First posted
2015-08-03
Last updated
2019-08-28
Results posted
2019-03-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02513940. Inclusion in this directory is not an endorsement.