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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 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.

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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.

Study Locations (1)

Massachusetts

  • Massachusetts General Hospital - Boston

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2021-01-21
Est. Completion 2026-03

Sponsor

Stephanie B. Seminara, MD

11 total trials

What the Registry Record Tells You About NCT05971836

The ClinicalTrials.gov registry entry for NCT05971836 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 27-participant average among 6 other Hypogonadotropic Hypogonadism trials with a reported enrollment target (2122% higher). The listed sponsor is Stephanie B. Seminara, MD, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Hypogonadotropic Hypogonadism appearing as the primary indexed condition, and to 0 interventions.

NCT05971836 reports 1 study location spanning 1 distinct geographic area - top geographies include 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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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