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NCT05971836 · ClinicalTrials.gov registry record
The Molecular Basis of Inherited Reproductive Disorders
A clinical trial of Hypogonadotropic Hypogonadism and Kallmann Syndrome, sponsored by Stephanie B. Seminara, MD.
- Recruiting
- Registry status
- 600
- Enrollment target
- 1
- Study location
NCT05971836: Recruiting study of Hypogonadotropic Hypogonadism and Kallmann Syndrome, sponsored by Stephanie B. Seminara, MD.
NCT05971836 is a study of Hypogonadotropic Hypogonadism and Kallmann Syndrome that is actively recruiting participants, run by Stephanie B. Seminara, MD. The registered enrollment target is 600 participants, above the 27-participant average among 6 other Hypogonadotropic Hypogonadism trials with a reported enrollment target (2122% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05971836, a study of Hypogonadotropic Hypogonadism and Kallmann Syndrome, is actively recruiting participants, sponsored by Stephanie B. Seminara, MD.
- RECRUITING
- Registry status
- 600 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this study is to learn more about the genes that control puberty and reproduction in humans.
Primary Outcome
Identification of one or more genetic variations related to reproductive disorders
Conditions Studied
Study Locations (1)
Massachusetts
- Massachusetts General Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2021-01-21 |
| Est. Completion | 2026-03 |
What NCT05971836 shows while recruiting
NCT05971836 is an observational study that tracks outcomes without assigning an intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, above the 27-participant average among 6 other Hypogonadotropic Hypogonadism trials with a reported enrollment target (2122% higher).
The record links to 4 conditions, with Hypogonadotropic Hypogonadism appearing as the primary indexed condition, and to 0 interventions.
NCT05971836 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT05971836 about?
NCT05971836 is a clinical study titled "The Molecular Basis of Inherited Reproductive Disorders". The goal of this study is to learn more about the genes that control puberty and reproduction in humans.
What is the current status of trial NCT05971836?
This trial is currently recruiting. The enrollment target is 600 participants. The study started on 2021-01-21. Estimated completion is 2026-03.
What conditions does trial NCT05971836 study?
This clinical trial studies the following conditions: Hypogonadotropic Hypogonadism, Kallmann Syndrome, Reproductive Disorder, Delayed Puberty.
Who is sponsoring clinical trial NCT05971836?
This trial is sponsored by Stephanie B. Seminara, MD, which has 11 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05971836 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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