Actively Recruiting
Evaluation of Clinical Outcomes and Acceptability of an Anatomical Classification for Placenta Accreta Spectrum
Led by University of California, Los Angeles · Updated on 2026-01-16
60
Participants Needed
1
Research Sites
160 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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 pregnant people with an a prior risk of PAS. The study will involve pregnant patients with PAS risk factor, include data collection spanning prenatal assessment, intraoperative classification, surgical technique implementation and postoperative analysis. The anticipated study duration is approximately 36-48 months.
CONDITIONS
Official Title
Evaluation of Clinical Outcomes and Acceptability of an Anatomical Classification for Placenta Accreta Spectrum
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 least one prenatal assessment before surgery
- Expected age range: 18-55
- Patient has agreed to conservative management approach as part of standard of care if feasible intraoperatively
You will not qualify if you...
- Patients who decline participation or withdraw consent
- Those with contraindications to the planned surgical procedure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of California, Los Angeles
Los Angeles, California, United States, 90095
Actively Recruiting
Research Team
D
Dana Levin-Lopez, MPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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