Sub Lingual Misoprostol Before IUD Insertion in Women With Only Previous Cesarean Section

IUD Insertion Clinical Trial

Official title:
SUB LINGUAL MISOPROSTOL PRIOR TO IUD INSERTION IN WOMEN WITH ONLY PREVIOUS CESARIAN SECTION: A Randomized Controlled Trial

Status Completed

Clinical Trial Summary

The aim of the work is to evaluate the efficacy of the sub lingual prostaglandin E1 synthetic analogue (misoprostol) before IUD insertion to facilitate the procedure in patients delivered before only by cesarean section.

Clinical Trial Description

The study will be conducted at Ain Shams University Maternity Hospital. 124 women candidate for Cu T 380A IUD insertion will be enrolled in the study. Half of them will receive 400 micro gram of misoprostol (Sigma) sub lingually and the other half will receive the placebo two hours before IUD insertion. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

IUD Insertion

Clinical Trial Details

NCT number	NCT02141321
Study type	Interventional
Source	Ain Shams University
Contact
Status	Completed
Phase	Phase 2/Phase 3
Start date	May 2014
Completion date	January 2015

View Details

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