LutrePulse Hypogonadotropic Hypogonadism
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.
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
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
To compare the ovulation rate in women with primary amenorrhea with hypogonadotropic hypogonadism following pulsatile gonadotropin-releasing hormone (GnRH) treatment using the OmniPod pump versus placebo
Study identification
- NCT ID
- NCT01976728
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- 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
- Apr 1, 2014 (Actual)
- Primary completion
- Feb 23, 2018 (Actual)
- Completion
- Feb 23, 2018 (Actual)
- Last update posted
- Mar 3, 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 3, 2021 · Synced Oct 24, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT01976728 live on ClinicalTrials.gov.