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Clinical Trial Summary

The purpose of this study is to compare trans-abdominal uterine massage to sustained uterine compression after vaginal delivery with respect to blood loss and maternal pain. It is a randomized controlled trial that will be conducted at the American University of Beirut Medical Center - Delivery Suite.


Clinical Trial Description

Women allocated to either the massage or compression group will be given 10 units of oxytocin intramuscularly immediately after delivery of the shoulder and controlled cord traction will be performed to assist placental delivery. The umbilical cord will be clamped and cut approximately 1 minute after delivery of the baby. The uterine fundus will be rubbed and blood clots expelled as quickly as possible after delivery of the placenta. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02396771
Study type Interventional
Source American University of Beirut Medical Center
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date October 2017

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