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COMPLETED Phase 2

Treating PCOS With Semaglutide vs Active Lifestyle Intervention

NCT03919929 · View on ClinicalTrials.gov ↗

Study Summary

Girls with obesity and polycystic ovarian syndrome will receive either glucagon like peptide-1 receptor agonist therapy or a dietary intervention for 12 weeks to decrease the metabolic syndrome, in particular to lower hepatic fat and improve insulin sensitivity.

Interventions

  • DRUG Semaglutide 3mg and 7mg [Rybelsus]
  • OTHER Weight loss diet

Study Locations (1)

Colorado

  • University of Colorado Anshutz Medical Campus/Children's Hospital Colorado — Aurora

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2019-05-03
Est. Completion 2023-10-03
Phase Phase 2

Sponsor

University of Colorado, Denver

1,447 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03919929

The ClinicalTrials.gov registry entry for NCT03919929 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Colorado, Denver, which has 1,447 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with NAFLD appearing as the primary indexed condition, and to 2 interventions — of which Semaglutide 3mg and 7mg [Rybelsus] is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03919929 reports 1 study location spanning 1 distinct geographic area — top geographies include Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03919929 about?

NCT03919929 is a clinical study titled "Treating PCOS With Semaglutide vs Active Lifestyle Intervention". Girls with obesity and polycystic ovarian syndrome will receive either glucagon like peptide-1 receptor agonist therapy or a dietary intervention for 12 weeks to decrease the metabolic syndrome, in particular to lower hepatic fat and improve insulin sensitivity.

What is the current status of trial NCT03919929?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2019-05-03. Estimated completion is 2023-10-03.

What conditions does trial NCT03919929 study?

This clinical trial studies the following conditions: NAFLD, Adolescent Obesity, PCOS. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03919929?

The interventions under investigation include: Semaglutide 3mg and 7mg [Rybelsus] (DRUG), Weight loss diet (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03919929?

This trial is sponsored by University of Colorado, Denver, which has 1,447 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03919929 being conducted?

This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial