Placenta Accreta Spectrum Topographic Classification

Last updated: February 10, 2025
Sponsor: Fundacion Clinica Valle del Lili
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT05922397
FVL-2125
  • Ages 18-55
  • Female
  • Accepts Healthy Volunteers

Study Summary

The present study is a prospective multicenter study consisting of a cohort of patients with prenatal or intraoperative diagnosis of PAS, evaluating the clinical outcomes of the group of patients found in each category of the topographic classification. In addition, an approach to evaluate the acceptability of this classification among the obstetrician-gynecologists of the participating medical centers will be included.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Pregnant woman over 18 years old.

  • Prenatal diagnosis by ultrasound or MRI of Placenta Accreta Spectrum (PAS),regardless of the suspected degree of severity of the disease.

  • Case requiring surgical management, either as scheduled or emergent procedure.

  • Application of the topographic classification of placenta accreta spectrum duringlaparotomy.

Exclusion

Exclusion Criteria:

  • None.

Study Design

Total Participants: 326
Study Start date:
May 21, 2023
Estimated Completion Date:
June 01, 2025

Study Description

The aim of this study is to describe the demographic and clinical characteristics of patients with a diagnosis of placenta accreta spectrum, and to determine the correlation between the topographic classification and the clinical outcomes found in the study. Finally, to evaluated whether the proposed classification is accepted by the obstetrician-gynecologists of the participating centers that manage placenta accreta spectrum patients.

It is an observational, multicentric study of a prospective cohort, in which data will be obtained from the medical records and other documents in each participating center, which are considered to be of routine use in day-to-day clinical practice. The study of the outcomes proposed in this protocol will be limited to those recorded in the clinical records and will be taken into account until the participant is discharged from the hospital, during which a surgical intervention was performed due to the suspicion or diagnosis of PAS.

It is projected that the period of patient enrollment will last 2 years, counting on from the first participant included. The study population is pregnant patients with a diagnosis of placenta accreta spectrum who visits any of the participating medical centers, and also obstetrician-gynecologists working in participating medical centers.

The centers invited to participate are hospitals or clinics that already have knowledge in how to apply the surgical staging of PAS, and the topographic classification and have experience using it.

Connect with a study center

  • Fundación Valle del Lili

    Cali,
    Colombia

    Active - Recruiting

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