NCT07250412

Brief Summary

To evaluate the correlation between preoperative ultrasound imaging findings by 3D Color Doppler Ultrasound and the intraoperative severity of Placenta Accreta Spectrum (PAS) disorders, in order to assess the diagnostic accuracy of sonographic markers and their utility in predicting the extent of placental invasion.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 10, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 10, 2025

Completed
20 days until next milestone

First Submitted

Initial submission to the registry

September 30, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

November 26, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

November 26, 2025

Status Verified

September 1, 2025

Enrollment Period

Same day

First QC Date

September 30, 2025

Last Update Submit

November 24, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Correlation between preoperative ultrasound findings and the confirmed degree of Placenta Accreta Spectrum (PAS) severity (classified as accreta, increta, or percreta). o The classification will be based on intraoperative surgical findings.

    Patient preg 28 wks compare finding intraoperative

  • Correlation between preoperative ultrasound findings and the confirmed degree of Placenta Accreta Spectrum (PAS) severity (classified as accreta, increta, or percreta). o The classification will be based on intraoperative surgical findings.

    Pt preg for more than 28wks preg and compare finding intraoperative

Study Arms (1)

Ultrasonography

ACTIVE COMPARATOR
Procedure: Cesarian section

Interventions

Cesarian section for detection the degree of placenta Accreta spectrum invasion comparaple to 3D color Doppler

Ultrasonography

Eligibility Criteria

Age16 Years - 45 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Placenta previa or low-lying placenta
  • History of previous cesarean section(s) or uterine surgery (e.g., myomectomy, D\&C) 2. Gestational age ≥ 28 weeks at the time of ultrasound evaluation 3. Undergoing planned cesarean delivery in the study hospital 4. Availability of preoperative ultrasound imaging performed using a standardized protocol.
  • \. Patient can provide informed Written consent and Agree to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of medecine Sohag university

Sohag, Egypt

Location

MeSH Terms

Interventions

Cesarean Section

Intervention Hierarchy (Ancestors)

Delivery, ObstetricObstetric Surgical ProceduresSurgical Procedures, Operative

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
The Accuracy Of 3D Color Ultrasonography for Detecting the degree of placenta Accreta spectrum invasion

Study Record Dates

First Submitted

September 30, 2025

First Posted

November 26, 2025

Study Start

September 10, 2025

Primary Completion

September 10, 2025

Study Completion

March 1, 2026

Last Updated

November 26, 2025

Record last verified: 2025-09

Locations