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Evaluation of Cervical Invasion and Length in Placenta Accreta Patients

NCT07452185 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-03-05

No results posted yet for this study

Summary

Placenta accreta spectrum (PAS), also called morbidly adherent placenta, is a serious pregnancy problem where the placenta attaches too deeply to the uterus wall and does not come out normally after birth. This often happens after previous cesarean sections or when the placenta is low (placenta previa). It can cause heavy bleeding, serious complications, and danger to the mother.

This study will look at pregnant women with PAS at Sohag University Hospital in Egypt. Researchers will use ultrasound to check two things:

How much the placenta has invaded the cervix (the lower part of the uterus). The length of the cervix.

The main goals are to find out:

How common cervical invasion is in PAS cases. What happens to women who have this invasion (outcomes like bleeding or surgery needs).

If a short cervix is linked to early labor (preterm birth). Women with confirmed PAS will join this observational study from March 2026 to January 2028. They will have extra ultrasound scans during pregnancy. No new treatments or drugs are tested - the study only collects information from routine care and scans to better understand the condition.

This research may help doctors predict risks earlier, plan safer deliveries, and improve care for mothers and babies with PAS in the future.

Conditions

  • Placenta Accreta Spectrum
  • Placenta Accreta
  • Placenta Previa

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Principal Investigators

  • Ahmed Salah Ali, MSC · Sohag University

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-01
Primary Completion
2028-01-01
Completion
2028-01-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07452185 on ClinicalTrials.gov