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Completed Phase 3 Interventional Results available

LutrePulse Hypogonadotropic Hypogonadism

ClinicalTrials.gov ID: NCT01976728

Public ClinicalTrials.gov record NCT01976728. 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, 3:13 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 Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism

Study identification

NCT ID
NCT01976728
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
39 participants

Conditions and interventions

Interventions

  • Gonadorelin acetate subcutaneous (SC) 10 μg/pulse as a fixed dose, administered via. OmniPod pump Drug
  • Gonadorelin acetate SC 15 μg/pulse as a fixed dose, administered via. OmniPod pump Drug
  • Gonadorelin acetate SC 20 μg/pulse as a fixed dose, administered via. OmniPod pump Drug
  • Placebo (SC 10, 15, or 20 μg/pulse as a fixed dose, administered via. OmniPod pump) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 40 Years
Sex
Female
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
Mar 31, 2014
Primary completion
Feb 22, 2018
Completion
Feb 22, 2018
Last update posted
Mar 2, 2021

2014 – 2018

United States locations

U.S. sites
33
U.S. states
22
U.S. cities
31
Facility City State ZIP Site status
Fertility Treatment Center Tempe Arizona
Center for Reproductive Health UCSF San Francisco California
University of Colorado School of Medicine Aurora Colorado
Reproductive Associates of Delaware Newark Delaware
Columbia Fertility Associates Washington D.C. District of Columbia
Women's Medical Research Group, LLC Clearwater Florida
Center for Reproductive Medicine Orlando Florida
Georgia Reproductive Specialists Atlanta Georgia
Fertility Centers of Illinois Chicago Illinois
Cypress Medical Research Center Wichita Kansas
Bluegrass Clinical Research Inc. Louisville Kentucky
Maine Medical Center-REI Portland Maine
Massachusetts General Hospital Boston Massachusetts
Wayne State University Physicians Group Southfield Michigan
Weill Cornell Medical College New York New York
Carolinas HealthCare System Charlotte North Carolina
Lyndhurst Clinical Research Winston-Salem North Carolina
Wake Forest University Health Sciences Winston-Salem North Carolina
Institute for Reproductive Health Cincinnati Ohio
University of Cincinnati Physicians Cincinnati Ohio
UH Case Medical Center, MacDonald Clinical Trials Cleveland Ohio
Ohio Reproductive Medicine Columbus Ohio
University of Oklahoma Health Sciences Center, Abington IVF & Genetics, L.P. Oklahoma City Oklahoma
Abington Reproductive Medicine, PC Abington Pennsylvania
Main Line Fertility Center Bryn Mawr Pennsylvania
Penn State MS Hershey Medical Center, Penn State College of Medicine Hershey Pennsylvania
University of Pittsburgh, Magee-Womens Hospital Pittsburgh Pennsylvania
Fertility Associates of Memphis PLLC Memphis Tennessee
Center for Assisted Reproduction Bedford Texas
Houston Fertility Institute Houston Texas
Center of Reproductive Medicine Webster Texas
Utah Fertility Center Pleasant Grove Utah
Jones Institute for Reproductive Medicine Norfolk Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01976728, 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 Mar 2, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01976728 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →