NCT03487185Active, not recruiting
Continuous Positive Airway Pressure (CPAP) for Sleep Apnea in Pregnancy
A Randomized Trial of Continuous Positive Airway Pressure (CPAP) for Sleep Apnea in Pregnancy
Source: ClinicalTrials.gov · Last updated 5 Aug 2026
Brief summary (registry, in English)
A randomized controlled trial of 1,500 women to assess whether treatment of obstructive sleep apnea with continuous positive airway pressure (CPAP) in pregnancy will result in a reduction in the rate of hypertensive disorders of pregnancy.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 1500 (estimated)
- First submitted
- 22 Mar 2018
- Start date
- 3 Aug 2018
- Primary completion date
- 31 Oct 2026
- Lead sponsor
- The George Washington University Biostatistics Center
- NCT number
- NCT03487185
What you commit to
- Study type: Interventional
- Planned participants: 1500
- From 3 Aug 2018 to the primary completion date, 31 Oct 2026
- 14 sites 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
- Previously prescribed, current or planned therapy for sleep apnea.
- Asthma requiring systemic steroid therapy for more than 14 days within the past 6 months because this population is expected to be unresponsive to CPAP therapy.
- Participation in this trial in a previous pregnancy. Patients who were screened in a previous pregnancy, but not randomized, may be included.
Other illness
- Chronic medical conditions requiring oxygen supplementation (e.g. pulmonary fibrosis, pulmonary hypertension, cystic fibrosis) because this population is expected to be unresponsive to CPAP therapy.
- Antiphospholipid antibody syndrome, because it would compromise the primary outcome diagnosis.
- Active vaginal bleeding (more than spotting) at the time of randomization.
- Active drug use, alcohol use, or unstable psychiatric condition.
- Participation in another interventional study that influences preeclampsia, hypertensive disorders of pregnancy, or GDM.
Lab values
- Chronic renal disease with serum creatinine \>1.3 mg/dL because the primary outcome would be pre-determined.
- History of medical complications such as:
- Active liver disease (acute hepatitis, chronic active hepatitis, persistently abnormal liver enzymes)
- Thrombocytopenia with platelet count \<100,000 because of the difficulty in assessing the primary outcome.
Age
- Age \< 18 years, because the rate of sleep apnea in this population is extremely low.
Other
- Inability to sleep in a stable place with access to the CPAP machine at least 5 nights per week.
- Current use of prescribed sleeping pills for insomnia.
- Known chromosomal, genetic, major malformations or fetal demise, or planned termination of pregnancy because inclusion would compromise evaluation of secondary neonatal outcomes.
- Known major uterine malformations associated with adverse pregnancy outcomes.
- Current use of opiates (heroin, methadone, or other daily opioid use) due to inaccuracy of the home sleep test and inefficiency of CPAP.
- Prenatal care or delivery planned at a non-network center where access to the complete electronic medical record will not be available to research staff.
Who the study is looking for
- Singleton gestation. Twin gestation reduced to singleton, either spontaneously or therapeutically, is not eligible unless the reduction occurred before 14 weeks project gestational age.
- Gestational age at randomization between 14 weeks 0 days and 21 weeks 6 days based on clinical information and evaluation of the earliest ultrasound.
- Diagnosis with mild to moderate OSA as defined by an AHI score ≥ 5 and \<30.
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (14)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Alabama Birmingham Coordinator of this site? Confirm its status | Birmingham | United States | Unknown status |
| University of North Carolina, Chapel Hill Coordinator of this site? Confirm its status | Chapel Hill | United States | Unknown status |
| Northwestern University Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Case Western Reserve-Metro Health Coordinator of this site? Confirm its status | Cleveland | United States | Unknown status |
| Ohio State University Hospital Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| University of Texas Medical Branch Coordinator of this site? Confirm its status | Galveston | United States | Unknown status |
| Baylor College of Medicine Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| University of Texas Houston Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| Columbia University Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Hospital of the University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Magee Women's Hospital of UPMC Coordinator of this site? Confirm its status | Pittsburgh | United States | Unknown status |
| Brown Univeristy Coordinator of this site? Confirm its status | Providence | United States | Unknown status |
| University of Utah Medical Center Coordinator of this site? Confirm its status | Salt Lake City | United States | Unknown status |
| Regents of the University of California San Francisco Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.