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NCT07871149Recruiting

PMOS in OSA Pilot Study

Metabolic Changes in PMOS Patients With Obstructive Sleep Apnea (OSA) Pilot Study

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

The goal of this study is to obtain pilot data investigating the effects of sleep apnea on mitochondrial function and cellular metabolism in Polyendocrine Metabolic Ovarian Syndrome (PMOS) patients.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
1 Oct 2026
Start date
Oct 2026
Primary completion date
Oct 2027
Lead sponsor
University of Chicago
NCT number
NCT07871149

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From Oct 2026 to the primary completion date, Oct 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current use of anti-coagulant medication

Other illness

  • Any history of bleeding disorders
  • Any underlying disease likely to limit life span and/or increase risk of interventions including cardiovascular disease (e.g. unstable angina, heart failure requiring hospitalization in the past 6 months, significant heart block or arrhythmias, NYHA Class\>2), pulmonary disease with dependence on oxygen or daily use of bronchodilators, cancer requiring treatment in the past 5 years unless the prognosis is considered good, active or chronic infection, thyroid disease and other endocrine disorders (e.g. Cushing syndrome, acromegaly), hepatitis or other chronic gastrointestinal disease (pancreatitis, inflammatory bowel disease), renal disease, significant anemia, recent surgery or significant abdominal surgery, major psychiatric or any eating disorder, acute coronary syndrome or stroke in the past 6 months

Lab values

  • Hemoglobin \<11.6 g/dL

Other

  • Regular adherent CPAP use per clinical guidelines
  • Currently pregnant, pregnant within the last year, or gave birth within the last year

Who the study is looking for

  • Women 18-40 years old
  • PMOS diagnosis
  • Sleep Apnea (AHI\>5) diagnosed by home sleep test (WatchPAT One)
  • BMI\< 50.0

Age in the registry: 18 years to 40 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.