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Clinical Trial Summary

The aim of this study is to evaluate the efficacy of intramuscular autologus platelet rich plasma on uterine wound healing after primary cesarean section


Clinical Trial Description

110 pregnant female undergoing primary prelabor CS will be randomized to two groups group A)autologus PRP will be prepared from participant venous blood collected from the participants' arm into a syringe primed with ACD-A. then it will be injected into uterus after closing uterine incision . Injection sites will be selected near the incision at evenly 20 different sites

group B)normal saline 0.9 will be injected into uterus after closing uterine incision . Injection sites will be selected near the incision at evenly 20 different sites. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03497325
Study type Interventional
Source Ain Shams University
Contact
Status Not yet recruiting
Phase Phase 2
Start date April 2018
Completion date December 2018

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