Comparison between the outcomes of adherent placenta encountered during emergencies and adherent placenta managed electively

Not Applicable

Recruiting

• Conditions: Placenta accreta; Reproductive Health and Childbirth - Fetal medicine and complications of pregnancy

• Registration Number: ACTRN12614000606684
• Lead Sponsor: Cairo University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-06-06
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

Suspected placenta accreta (In the labour ward placenta accrete will be suspected by the grey scale ultrasound and colour Doppler. In women presenting electively, 3D ultrasound or MRI may be used for further confirmation)
-consent to participate in the study

Exclusion Criteria

-Intra uterine fetal death.
-Preeclampsia, Diabetes Mellitus or other medical disorders.
- Boby mass index (BMI)>35
-Known coagulation defects

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Eestimated blood loss during surgery.<br> The amount of blood in the suction container (which represents the amount of blood sucked from the surgical field) will be added to that staining the surgical towels and the sum will represent the estimated blood loss during surgery. [5 minutes after the Cesarean section ]

Secondary Outcome Measures

Name	Time	Method
surgical complications like injury to the bowel, bladder or ureters[5 minutes after completion of surgery];the need for admission to the intensive care unit[24 hours after surgery];Postoperative hospital stay[one week after the surgery];Need for hysterectomy[5 minutes after surgery];Need for blood transfusion[ 1 hour after surgery]