Skip to main content
Clinical Trials/NCT03032770
NCT03032770
Completed
Not Applicable

Early Prediction of Placenta Accreta by 2 Dimensional Transvaginal Ultrasound and Color Doppler

Assiut University1 site in 1 country148 target enrollmentJanuary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Placenta Accreta
Sponsor
Assiut University
Enrollment
148
Locations
1
Primary Endpoint
Confirmation of occurrence of placenta accreta during delivery.
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Placenta accreta is a substantially life threatening condition and one of the causes of maternal morbidity and mortality in the world. According to study done in United Kingdom, The estimated incidence of placenta accreta/increta/percreta was 1.7 per 10,000 maternities overall and 577 per 10,000 in women with both a previous cesarean delivery and placenta previa. in a tertiary south Italian center, The incidence increased from 0.12% during the 1970s, to 0.31% during the 2000s.While in United States of America, the prevalence of placenta accreta was 3.7 per 1000 deliveries.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
March 31, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Mohamed Abbas

clinical professor

Assiut University

Eligibility Criteria

Inclusion Criteria

  • Low implantation of the gestational sac (\<4 cm from external os) by transvaginal ultrasound
  • Presence of placental lakes by transvaginal ultrasound
  • Disruption of placental-myometrial interface by transvaginal ultrasound
  • Trophoblast overlapping a uterine scar (Cesarean section, myomectomy) by transvaginal ultrasound
  • Intraplacental dilated vessels by Doppler ultrasound
  • Turbulent blood flows by Doppler ultrasound
  • Greatly increased periplacental vascularity by Doppler ultrasound

Exclusion Criteria

  • a) Cases far away from our hospital and expected to be lost to be followed. b) Pregnant women who will refuse to Participate

Outcomes

Primary Outcomes

Confirmation of occurrence of placenta accreta during delivery.

Time Frame: duration of pregnancy

Study Sites (1)

Loading locations...

Similar Trials