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EFFICACY OF VAGINAL MISOPROSTOL AND CERVICAL FOLEY CATHETER VERSUS VAGINAL MISOPROSTOL ALONE ON TERM PREGNANCY LABOUR INDUCTION IN ENUGU: A RANDOMIZED CONTROLLED TRIA

Phase 3
Conditions
Fetomaternal
Registration Number
PACTR202202769135894
Lead Sponsor
Dr. Ezenwaeze Malachy Nwaeze
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
132
Inclusion Criteria

Every pregnant woman billed for labour induction at term (37 completed weeks to 41weeks + 6days gestation) with an unfavourable cervix (Bishop score of< 6) who gave consent, with live singleton fetus in longitudinal lie, cephalic presentation and reactive non-stress test will be selected.

Exclusion Criteria

Pregnant women at term who fail to give consent, with contraindication to vaginal delivery, multiple gestation, intrauterine fetal death, anomalous fetus, nonreactive stress test, prior uterine rupture/surgery, regular uterine contraction, vaginal bleeding, and premature rupture of membranes will be excluded.

Study & Design

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