Evaluation of Clinical Outcomes and Acceptability of an Anatomical Classification for Placenta Accreta Spectrum
Recruiting
Observational Study
Placenta Accreta
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 55
- Sex
- Female
- Study type
- Observational
- Participants needed
- 60 (estimated)
- Sponsor
- University of California, Los Angeles · Other
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About This Trial
This study evaluates the clinical implementation of intra-operative topographic classification system for PAS. In addition to a standard of care risk stratification prenatal ultrasound for patients with a risk of PAS, this study adds an additional intraoperative surgical staging protocol to validate the classification system, improve surgical approach, and significantly clinical outcomes of pregna…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant people suspected of having PAS based on ultrasound findings or clinical risk factors
* Patients undergoing planned surgical intervention for PAS, including a planned cesarean
* Individuals who provide informed consent to participate in the study
* Patients with at lea…
Contacts