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Completed Phase 1 Interventional Accepts healthy volunteers

Effect of Udenafil on Spermatogenesis

ClinicalTrials.gov ID: NCT01230541

Public ClinicalTrials.gov record NCT01230541. 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.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Effect of Udenafil on Spermatogenesis: A Double-blind, Randomized, Placebo-controlled, Parallel-group Study

Study identification

NCT ID
NCT01230541
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Warner Chilcott
Industry
Enrollment
239 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Udenafil Drug

Drug

Eligibility (public fields only)

Age range
25 Years to 64 Years
Sex
Male
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2010
Primary completion
Oct 31, 2011
Completion
Oct 31, 2011
Last update posted
Nov 29, 2011

2010 – 2011

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
22
Facility City State ZIP Site status
Warner Chilcott Investigational Site Huntsville Alabama 35801
Warner Chilcott Investigational Site Anaheim California 92801
Warner Chilcott Investigational Site San Diego California 92103
Warner Chilcott Investigational Site San Diego California 92120
Warner Chilcott Investigational Site Tarzana California 91356
Warner Chilcott Investigational Site Middlebury Connecticut 06762
Warner Chilcott Investigational Site Aventura Florida 33180
Warner Chilcott Investigational Site Clearwater Florida 33759
Warner Chilcott Investigational Site Doral Florida 33166
Warner Chilcott Investigational Site Ocala Florida 34474
Warner Chilcott Investigational Site Pinellas Park Florida 33782
Warner Chilcott Investigational Site Atlanta Georgia 30342
Warner Chilcott Investigational Site Shreveport Louisiana 71115
Warner Chilcott Investigational Site Plainsboro New Jersey 08536
Warner Chilcott Investigational Site Garden City New York 11530
Warner Chilcott Investigational Site Great Neck New York 11021
Warner Chilcott Investigational Site Purchase New York 10577
Warner Chilcott Investigational Site Williamsville New York 14221
Warner Chilcott Investigational Site Cincinnati Ohio 45212
Warner Chilcott Investigational Site San Antonio Texas 78229
Warner Chilcott Investigational Site Webster Texas 77598
Warner Chilcott Investigational Site Norfolk Virginia 23507
Warner Chilcott Investigational Site Spokane Washington 99204

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 NCT01230541, 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 Nov 29, 2011 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01230541 live on ClinicalTrials.gov.

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