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Completed Phase 2 Interventional Results available

Normalization of Morning Testosterone Levels in Men With Secondary Hypogonadism

ClinicalTrials.gov ID: NCT01270841

Public ClinicalTrials.gov record NCT01270841. 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 Sep 2, 2026, 12:38 AM 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 and Active Controlled, Parallel, Multi-Center Phase IIb Study to Evaluate Normalization of Morning Testosterone Levels in Men With Secondary Hypogonadism

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The Purpose of the study is to determine the effects of Androxal on morning testosterone and reproductive status in men with secondary hypogonadism(confirmed morning Testosterone less than 250 ng/dL), compared to changes with placebo, or Testim (topical testosterone). The effects of Testim versus placebo on reproductive status will also be examined. Study subjects must not be currently using a topical testosterone.

Study identification

NCT ID
NCT01270841
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Repros Therapeutics Inc.
Industry
Enrollment
83 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years to 65 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
Dec 31, 2010
Primary completion
Nov 30, 2011
Completion
Nov 30, 2011
Last update posted
Jul 27, 2014

2011

United States locations

U.S. sites
18
U.S. states
4
U.S. cities
14
Facility City State ZIP Site status
Paradigm Clinical Inc. Garden Grove California 92844
Northern California Research Corp Sacramento California 95831
Medical Center for Clinical Research San Diego California 92108
Los Angeles Biomedical Research Institute Torrance California 90502
Affiliated Clinical Research Las Vegas Nevada 89109
Affiliated Clinical Research Inc. Las Vegas Nevada 89144
Weill Cornell Medical College and Smith Institute Great Neck New York 11021
Jed Kaminetsky New York New York 10016
Natan Bar-Chama New York New York 10022
Michael A Werner Purchase New York 10577
Discovery Clinical Trials Austin Texas 78758
Research Across America Carrollton Texas 75010
Texas Urology Specialist Houston Texas 77024
Centex Research Houston Texas 77062
Endocrine and Psychiatry Center Houston Texas 77095
Protenium Clinical Research Hurst Texas 76054
R/D Clinical Research Lake Jackson Texas 77566
Cetero Research San Antonio Texas 78229

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 NCT01270841, 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 Jul 27, 2014 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01270841 live on ClinicalTrials.gov.

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