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Completed Phase 3 Interventional Results available

Phase III Study to Evaluate Morning Testosterone Normalization in Overweight Men With Secondary Hypogonadism

ClinicalTrials.gov ID: NCT01739595

Public ClinicalTrials.gov record NCT01739595. 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 22, 2026, 5:54 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

A Randomized, Double Blind, Placebo Controlled Multi-Center Phase III Study to Evaluate Normalization of Morning Testosterone Levels in Overweight Men With Acquired Hypogonadotropic Hypogonadism and Normal Sperm Concentration

Study identification

NCT ID
NCT01739595
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Repros Therapeutics Inc.
Industry
Enrollment
181 participants

Conditions and interventions

Interventions

  • enclomiphene citrate Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 60 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
Oct 31, 2012
Primary completion
Aug 31, 2013
Completion
Aug 31, 2013
Last update posted
May 26, 2015

2012 – 2013

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Coastal Clinical Research Mobile Alabama 36608
Baptist Health Center for Clinical Research Little Rock Arkansas 72205
Rancho Cucamonga Clinical Trials Rancho Cucamonga California 91730
Meridien Research Bradenton Florida 34208
All Medical Research Cooper City Florida 33024
Clinical Research of South Florida Coral Gables Florida 33134
Phase One Solutions Miami Gardens Florida 33169
Central Kentucky Research Associates Lexington Kentucky 40509
Rochester Clinical Research Rochester New York 14609
Coastal Carolina Research Center Mt. Pleasant South Carolina 29464
New Orleans Center for Clinical Research Knoxville Texas 37920
Lone Peak Family Medicine Draper Utah 84020
Granger Medical Clinic Riverton Utah 84065

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 NCT01739595, 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 May 26, 2015 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01739595 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →