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NCT04993651
Effect of CPAP on Fetal pH at Scheduled C-section in Morbidly Obese Women
NA trial testing CPAP in Morbid Obesity in 66 participants. Completed in 30 June 2023.
9 May 2023
Quick facts
| Lead sponsor | Eastern Virginia Medical School |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 66 |
| Start date | 11 October 2021 |
| Primary completion | 9 May 2023 |
| Estimated completion | 30 June 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- CPAP
Conditions studied
- Morbid Obesity — all drugs for Morbid Obesity →
- Cesarean Delivery Affecting Fetus — all drugs for Cesarean Delivery Affecting Fetus →
Sponsor
Eastern Virginia Medical School
Who can join
Adults 18 to 45, female only, with Morbid Obesity or Cesarean Delivery Affecting Fetus. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective of our study is to evaluate the effect of CPAP on umbilical cord acid base status in morbidly obese women at the time of scheduled cesarean delivery. We hypothesize that neonates born to mothers wearing CPAP during the cesarean section will have a higher umbilical artery pH.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04993651
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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- NCT07246538 — Positive Airway Pressure (PAP) System Evaluation in Volunteers · NA · not yet recruiting
Other recruiting trials for Morbid Obesity
Currently open trials in the same condition.
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Other Eastern Virginia Medical School trials
Trials by the same sponsor.
- NCT07224893 — Once-Daily vs Twice-Daily Insulin Glargine in Pregestational Diabetes Management · Phase 4 · not yet recruiting
- NCT07119398 — Oxytocin/Foley vs. Oxytocin for Induction in Patients With PPROM · Phase 4 · recruiting
- NCT06867861 — Effect of Fiber Supplementation on the Need for Medication With Gestational Diabetes · NA · recruiting
- NCT06274398 — Rectal Insert TAF/EVG Pre-Exposure Prophylaxis (RITE PrEP) Study · Phase 1 · completed
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04993651 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Eastern Virginia Medical School
- Last refreshed: 19 September 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04993651.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing