Misoprostol for Reduction of Blood Loss During Fibroid Surgery

Status Terminated

Clinical Trial Summary

The aim of this research work is to assess the impact of a single preoperative dose of buccal misoprostol in reducing blood loss during abdominal fibroid surgery.

Clinical Trial Description

This is a trial of women undergoing fibroid surgery at a university-affiliated tertiary care center. Eligible participants will be randomized to receive preoperative 400ucg buccal (under the tongue) misoprostol or placebo on the basis of total fibroid volume, location, parity. Intra-operative blood loss will be compared between groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02209545
Study type	Interventional
Source	Northwestern University
Contact
Status	Terminated
Phase	Phase 4
Start date	October 2014
Completion date	July 2022

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See also
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