Actively Recruiting

Age: 18Years - 55Years
FEMALE
ID07283042

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

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a topographic classification system for placenta accreta spectrum (PAS) to improve surgical planning and outcomes. This prospective cohort study focuses on the clinical use of an intraoperative staging protocol alongside prenatal ultrasound to better classify PAS and guide surgical decisions. The study aims to validate the classification system by comparing ultrasound findings with intraoperative and postoperative data, while also exploring biomarkers linked to PAS severity. Participants are pregnant individuals at risk for PAS undergoing planned surgical interventions such as total hysterectomy, modified subtotal hysterectomy, or one-step conservative surgery. The study integrates prenatal ultrasound staging with intraoperative classification to inform real-time surgical management. Data collected will include surgical details, photos, videos, blood loss measurements, and pathological examination of tissues. Optional serial blood draws will be stored in a biorepository for biomarker analysis. During the study, participants will undergo ultrasound assessments within 30 days before surgery and intraoperative evaluation during the procedure. Blood loss will be documented throughout surgery, and tissue analysis will occur within two hours post-surgery. Researchers will monitor adverse events for up to 12 months after surgery. The anticipated study duration is approximately 36 to 48 months, covering prenatal assessment, surgery, and follow-up evaluations.

CONDITIONS

Brief Title

Evaluation of Clinical Outcomes and Acceptability of an Anatomical Classification for Placenta Accreta Spectrum

Who Can Participate

Age: 18Years - 55Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant people suspected of having placenta accreta spectrum based on ultrasound findings or clinical risk factors
  • Patients undergoing planned surgical intervention for placenta accreta spectrum, 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 years
  • Patient has agreed to conservative management approach as part of standard of care if feasible intraoperatively
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 30 days prior to planned surgery

Participants undergo ultrasound assessments to evaluate placenta accreta spectrum and plan surgical intervention.

1 to 2 visits depending on ultrasound scheduling

Surgery and Immediate Post-operative Care

Duration - Day of planned surgery

Participants receive planned surgical intervention for placenta accreta spectrum with intraoperative staging and classification guiding surgical decisions.

1 surgical visit (in-person)

Post-operative Follow-up

Duration - Up to 12 months post surgery

Participants are monitored for clinical outcomes including adverse events and recovery up to 12 months after surgery.

Approximately 6 post-operative visits

Trial Site Locations

Total: 1 location

1

University of California, Los Angeles

Los Angeles, California, United States, 90095

Actively Recruiting

Loading map...

Research Team

D

Dana Levin-Lopez, MPH

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

Similar Trials

3D Ultrasound Placental Volume and Vascular Indices Versus 2...

Placenta Accreta

Actively Recruiting

1 location

Diagnosis and Outcomes of Placental Accretism

Placenta Accreta

Actively Recruiting

7 locations

Evaluation of Clinical Outcomes and Acceptability of an Anat...

Placenta Accreta

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here