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Traction effect with folly catheter on cervices ripening compared to vaginal misoprostol

Not Applicable
Conditions
Cervical ripening.
Encounter for full-term uncomplicated delivery
Registration Number
IRCT20170326033142N2
Lead Sponsor
Sanandaj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

Women referring to the delivery block of Besat Hospital indicating the induction of labor.
Gestational age equal to or greater than 37 weeks
Satisfaction to participate in the research
intact chorionic membrane
Vortex presentation
Single pregnancy
Inappropriate cervix and Bishop score 1 equal to or less than 4

Exclusion Criteria

fetal distress
Problems in controlling fetal heart sounds
severe pre-eclampsia
Intrauterine growth restriction
Contraindications for the use of prostaglandins
Regular uterine contractions
Early placental detachment
Placenta previa
Vaginal bleeding
Previous cesarean section or previous surgery on the uterus

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dilation. Timepoint: Every 1 hour. Method of measurement: Vaginal examination.;Effacement. Timepoint: Every 1 hour. Method of measurement: Vaginal examination.;Delivery progress time. Timepoint: Every 1 hour. Method of measurement: Vaginal examination.
Secondary Outcome Measures
NameTimeMethod
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