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Diagnostic Accuracy of a Specialized Pro Forma in Assessing Morbidly Adherent Placenta With Correlation to Intra-operative Findings

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Morbidly Adherent Placenta

Treatments

Diagnostic Test: Ultrasound

Study type

Observational

Funder types

Other

Identifiers

NCT04938050
23-2021

Details and patient eligibility

About

This study objective is to assess the accuracy of a specialized pro forma in suggesting the probability of Morbidly Adherent Placenta, its extent and its correlation with intraoperative findings.

Enrollment

21 estimated patients

Sex

Female

Ages

28 to 42 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age group 28:42 years.
  • Pregnant women in their late third trimester (34 0/7 weeks: 37 0/7 weeks).
  • With a single living fetus in the current pregnancy.
  • A previous delivery by at least 1 cesarean section or history of uterine surgery including (surgical evacuation, myomectomy or endometrium ablation)
  • Having an anterior placenta previa or anterior low-lying placenta by ultrasound assessment.

Exclusion criteria

  • Cases with a non-previa placenta, posterior low lying placenta or posterior previa placenta.
  • Maternal chronic medical disorders( diabetes mellitus, hypertension)
  • Patients presented with severe attack of bleeding.
  • Patients presented with rupture of membrane.
  • Emergency delivery regardless the cause.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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