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Comparison of reduction of blood loss at myomectomy using Misoprostol to that of Haemostatic Torniquet

Not Applicable
Completed
Conditions
Fertility-female
Uterine Fibroid
Registration Number
PACTR201802003039106
Lead Sponsor
niversity of Ilorin Teaching Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

Diagnosis of uterine fibroid with a treatment plan for abdominal myomectomy

Exclusion Criteria

1.Known allergy to prostaglandins including misoprostol.
2.Chronic medical disorders including hypertension, diabetes mellitus, cardiac or pulmonary diseases.
3.Previous uterine surgery (myomectomy or caesarean section).
4.Known bleeding or clotting disorders.
5.Haematocrit at 24hours before surgery less than 30%.
6.Patient refusal to participate in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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