Exploratory Study of Pagoclone in Men With Premature Ejaculation.
Public ClinicalTrials.gov record NCT00370981. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Four-arm, Randomized, Double-blind, Parallel, Placebo-controlled Exploratory Study of Pagoclone 0.15mg, 0.30mg, and 0.60mg in Men With Primary Premature Ejaculation.
Study identification
- NCT ID
- NCT00370981
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2
- Lead sponsor
- Endo USA Inc., a Keenova Therapeutics Company
- Industry
- Enrollment
- 100 participants
Conditions and interventions
Conditions
Interventions
- pagoclone Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years to 55 Years
- Sex
- Male
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jun 30, 2006
- Primary completion
- Jun 30, 2006
- Completion
- Sep 30, 2006
- Last update posted
- Dec 26, 2013
2006
United States locations
- U.S. sites
- 16
- U.S. states
- 11
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Urology Centers of Alabama, PC | Homewood | Alabama | 35209 | — |
| SD Uro-Research | San Diego | California | 92103 | — |
| Urology Research Options | Aurora | Colorado | 80012 | — |
| Urology Associates, PC | Denver | Colorado | 80210 | — |
| Connecticut Clinical Research Center | Waterbury | Connecticut | 06708 | — |
| South Florida Medical Research | Aventura | Florida | 33180 | — |
| Northeast Indiana Research, LLC | Fort Wayne | Indiana | 46825 | — |
| Davis Clinic, PC | Indianapolis | Indiana | 46202 | — |
| Regional Urology, LLC | Shreveport | Louisiana | 71106 | — |
| AccuMed Research Associates | Garden City | New York | 11530 | — |
| Urological Surgeons of Long Island, PC | Garden City | New York | 11530 | — |
| Center for Urologic Research of WNY | Williamsville | New York | 14221 | — |
| Metrolina Urology Clinic | Charlotte | North Carolina | 28207 | — |
| Wake Research Associates, LLC | Raleigh | North Carolina | 27612 | — |
| Johnny B. Roy, MD Private Practice | Edmond | Oklahoma | 73034 | — |
| Mobley Research Center | Houston | Texas | 77024 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00370981, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Dec 26, 2013 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00370981 live on ClinicalTrials.gov.