Control of Blood Loss During Caesarean Section

Status Completed

Clinical Trial Summary

trial of 3 protocols to determine the best one to control blood loss during caesarean section

Clinical Trial Description

The study population will be divided into 3 groups each containing 200 women:

Group (A): 200 patients will receive 5-IU oxytocin bolus over 3 minutes after delivery of the baby.

Group (B): 200 patients will receive 5-IU oxytocin bolus over 3 minutes and 30-IU oxytocin infusion in 500 ml 0.9 % saline over 4 hours after delivery of the baby.

Group (C): 200 patients will receive misoprostol 800 micrograms intrauterine, placed manually on the bottom of the uterine cavity after delivery of the placenta and cleaning of the cavity.

Operative blood loss will be estimated in theatre based on the volume in the suction bottle and the weight of swabs used. We will record blood loss up until the time the woman will be discharged from the theatre recovery ward.

Hemoglobin level and haematocrit value will be done as follow:-

1. After admission of each case in the pre-operative period.

2. Immediately post- operative.

3. 24 hours post- operative. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention

Related Conditions & MeSH terms

Complications; Cesarean Section

Clinical Trial Details

NCT number	NCT01412073
Study type	Interventional
Source	Cairo University
Contact
Status	Completed
Phase	Phase 3
Start date	September 2011
Completion date	October 2014

View Details

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