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Preoperative Vaginal Dinoprostone Versus Misoprostone in Abdominal Myomectomy

Myoma;Uterus Clinical Trial

Official title:
Preoperative Vaginal Dinoprostone Versus Misoprostone to Decrease Bleeding During Abdominal Myomectomy

Clinical Trial Summary

Aim and objectives; To compare the efficacy of preoperative administration of dinoprostone 20 mg versus 400 ug misoprostol vaginally in decreasing the amount of bleeding during abdominal myomectomy

Clinical Trial Description

Background; Myomectomy is a curative interventional option for many kinds of uterine fibroids, but considerable intraoperative haemorrhage and the necessities for transfusions of blood are still the main challenge for abdomen myomectomy. Aim and objectives; To compare the efficacy of preoperative administration of dinoprostone 20 mg versus 400 ug misoprostol vaginally in decreasing the amount of bleeding during abdominal myomectomy Subjects and methods; This was a prospective randomized double-blind controlled study that included 90 patients complaining of uterine myoma and indicated for myomectomy selected from the outpatient clinic at Beni-suef university hospital ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05761418
Study type Interventional
Source Beni-Suef University
Contact
Status Completed
Phase Phase 3
Start date March 1, 2018
Completion date February 20, 2023
View Details
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