Overview

Single Versus Double Dose Intra-vaginal Prostaglandin E2 "Misoprostol" Prior Abdominal Myomectomy

Status:
Completed
Trial end date:
2013-01-01
Target enrollment:
0
Participant gender:
Female
Summary
Introduction: The study aimed to investigate the effectiveness of a single versus double dose of Prostaglandin E2 "Misoprostol, 400 microgram" during myomectomy for multiple uterine fibroids. This was a prospective randomized controlled trial comprised of 69 patients with multiple myomas undergoing myomectomy. Patients randomly allocated to either an intra-vaginal single dose of 400 microgram Misoprostol 1 hour pre-operatively (group A, 34 cases) or 2 doses, 3 and 1 hours, prior surgery (group B, 35 cases). Operation time, intra and post-operative blood loss, hemoglobin concentration, blood pressure and body's temperature were estimated and compared in both groups.
Phase:
Phase 4
Details
Lead Sponsor:
Mansoura University
Treatments:
Dinoprostone
Misoprostol
Criteria
Inclusion Criteria:

- All patients had symptomatic multiple uterine fibroids (abnormal vaginal bleeding,
lower abdominal dull aching pain and pelvic heaviness, subfertility or recurrent
abortion)

Exclusion Criteria:

- hypertension, cardiac and pulmonary disease, chronic endocrine or metabolic diseases
such as diabetes, obesity (body mass index >30 kg/m2), all cases of single myoma and
those known to be allergic to prostaglandin preparations.