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Completed Phase 3 Interventional

Assessment of the Effects of Enclomiphene Citrate on Bone Mineral Density in Men With Secondary Hypogonadism

ClinicalTrials.gov ID: NCT01619683

Public ClinicalTrials.gov record NCT01619683. 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, 3:22 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 12 Month, Single Blind, Placebo Controlled, Phase III Study to Assess the Effects of Enclomiphene Citrate Treatment On Bone Mineral Density in Men With Secondary Hypogonadism

Study identification

NCT ID
NCT01619683
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Repros Therapeutics Inc.
Industry
Enrollment
300 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
Aug 31, 2012
Primary completion
Aug 31, 2014
Completion
Aug 31, 2014
Last update posted
Sep 30, 2014

2012 – 2014

United States locations

U.S. sites
17
U.S. states
8
U.S. cities
17
Facility City State ZIP Site status
Not listed Mesa Arizona 85213
Not listed Phoenix Arizona 85050
Not listed Tempe Arizona 85283
Not listed Mission Viejo California 92691
Not listed Newport Beach California 92663
Not listed Rancho Cucamonga California 91730
Not listed Clearwater Florida 33761
Not listed Fort Lauderdale Florida 33308
Not listed Jupiter Florida 33458
Not listed Miami Florida 33143
Not listed Miami Gardens Florida 33169
Not listed Henderson Nevada 89052
Not listed Lawrenceville New Jersey 08690
Not listed New York New York 10016
Not listed Rochester New York 14609
Not listed Houston Texas 77030
Not listed Salt Lake City Utah 84124

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 NCT01619683, 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 Sep 30, 2014 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01619683 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →