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Exploratory Study of Pagoclone in Men With Premature Ejaculation.

Phase 2
Completed
Conditions
Premature Ejaculation
Interventions
Registration Number
NCT00370981
Lead Sponsor
Endo Pharmaceuticals
Brief Summary

The purpose of this study is to evaluate pagoclone in the treatment of premature ejaculation.

Detailed Description

The primary objective of this study is to evaluate the effect of 3 dose levels of pagoclone (0.15 mg, 0.30 mg, and 0.60 mg) versus placebo on intravaginal ejaculation latency time (IELT) male patients with primary premature ejaculation.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
100
Inclusion Criteria
  • A male regularly experiencing premature ejaculation
  • 18 to 55 yrs old
  • In a Stable relationship with one woman for at least 6 months
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PBOpagoclone-
0.15 mgpagoclone-
0.60 mgpagoclone-
0.30 mgpagoclone-
Primary Outcome Measures
NameTimeMethod
Intravaginal ejaculation latency time (IELT)
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (16)

Urology Centers of Alabama, PC

🇺🇸

Homewood, Alabama, United States

SD Uro-Research

🇺🇸

San Diego, California, United States

Urology Research Options

🇺🇸

Aurora, Colorado, United States

Urology Associates, PC

🇺🇸

Denver, Colorado, United States

Connecticut Clinical Research Center

🇺🇸

Waterbury, Connecticut, United States

South Florida Medical Research

🇺🇸

Aventura, Florida, United States

Northeast Indiana Research, LLC

🇺🇸

Fort Wayne, Indiana, United States

Davis Clinic, PC

🇺🇸

Indianapolis, Indiana, United States

Regional Urology, LLC

🇺🇸

Shreveport, Louisiana, United States

AccuMed Research Associates

🇺🇸

Garden City, New York, United States

Scroll for more (6 remaining)
Urology Centers of Alabama, PC
🇺🇸Homewood, Alabama, United States

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