Effect of Alpha Lipoic Acid on Uterine Scar Healing After Cesarean Section

Status Completed

Clinical Trial Summary

The aim of this study is to evaluate the efficacy of alpha lipoic acid on uterine scar healing after cesarean section by using saline contrast sonohysterography

Clinical Trial Description

This is a triple blind randomized placebo controlled prospective clinical trial that will be conducted in Ain Shams University Maternity Hospital.

in which a consecutive series of participant attending emergency room 102 women undergoing cesarean section for the first time will be randomized into two groups.

Group A (Study group): 51 women will receive alpha lipoic acid drug ( 600 mg twice daily) for 6 weeks after cesarean section and saline sonohysterography will be done after that.

Group B (Control group): 51 women will receive a placebo drug twice daily for 6 weeks after cesarean section and saline sonohysterography will be done after that. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03257514
Study type	Interventional
Source	Ain Shams University
Contact
Status	Completed
Phase	Phase 2
Start date	June 1, 2017
Completion date	February 1, 2018

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