Status:
COMPLETED
A Study to Evaluate Intravaginal Ejaculation Time in Men With and Without Premature Ejaculation
Lead Sponsor:
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Conditions:
Erectile Dysfunction
Eligibility:
MALE
18+ years
Brief Summary
The purpose of the study is to characterize intravaginal ejaculatory latency time (time between the start of vaginal intercourse and the start of intravaginal ejaculation) in men with and without prem...
Detailed Description
This is a multinational, multicenter, observational study in men with and without PE. The study consists of three visits: one visit for screening and enrollment, and two visits for observation after 1...
Eligibility Criteria
Inclusion
- Must be in a stable, monogamous, sexual relationship with the same woman (18 years of age or older) for at least 6 months, who plan to maintain their relationship for the duration of the study
- Must be in good general health
- Patient and partner willing to avoid situations or activities that may have an effect on their sexual activity (eg, refrain from any preplanned surgery)
Exclusion
- Has history of drug abuse within the past 2 years
- Has history of or current major psychiatric disorder such as mood disorders, anxiety disorders, schizophrenia, other psychotic disorders, or alcoholism
- Must have erectile dysfunction
- Patient who has decreased interest in sexual intercourse or has other forms of sexual dysfunction
- Patient whose partner has decreased interest in sexual intercourse, painful intercourse, or other forms of female sexual dysfunction
- Patient whose partner is more than 3 months pregnant
Key Trial Info
Start Date :
March 1 2005
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2005
Estimated Enrollment :
1115 Patients enrolled
Trial Details
Trial ID
NCT00210678
Start Date
March 1 2005
End Date
September 1 2005
Last Update
October 10 2012
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