Clinical Trials Directory

Trials / Completed

CompletedNCT00211094

A Study of the Effectiveness and Safety of Dapoxetine in the Treatment of Men With Premature Ejaculation

A Placebo-Controlled, Double-blind, Randomized, Parallel Study of the Efficacy and Safety of Dapoxetine HCl in the Treatment of Rapid Ejaculation

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
1,320 (actual)
Sponsor
Alza Corporation, DE, USA · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of the study is to demonstrate that dapoxetine can prolong intravaginal ejaculatory latency time (IELT) compared with placebo in men with premature ejaculation (PE).

Detailed description

One form of male sexual dysfunction is premature ejaculation (PE), which is also referred to as rapid ejaculation (RE). The study consists of 2 phases: pre-randomization phase (a screening visit and a 2-week baseline period); 12-week double-blind treatment phase during which patients will receive one of 2 doses of dapoxetine or placebo for use on an "as-needed" basis. The total duration of the study is approximately 14 weeks. Assessments of effectiveness include the average intravaginal ejaculatory latency time (as measured by stopwatch) during sexual intercourse, during the treatment period; control over ejaculation, participant and partner satisfaction with sexual intercourse, participant overall impression of change and severity of symptoms, based on questions asked at monthly intervals through the treatment phase. Safety assessments include the incidence, severity, and type of adverse events during the study, ECGs, as well as laboratory tests. At the end of the baseline period, patients from selected study centers will undergo blood sampling and ECG monitoring before and after the first dose of study medication. The study hypothesis is that treatment for 12 weeks with dapoxetine prolongs intravaginal ejaculatory latency time, compared with placebo, in men with PE. Oral tablets of dapoxetine (30 milligrams \[mg\] or 60mg) or placebo taken as needed during 12 weeks of treatment. No more than 1 dose within a 24-hour period.

Conditions

Interventions

TypeNameDescription
DRUGDapoxetine

Timeline

Completion
2004-06-01
First posted
2005-09-21
Last updated
2011-02-11

Source: ClinicalTrials.gov record NCT00211094. Inclusion in this directory is not an endorsement.