Clinical trial
Cervical Ripening Balloon Compared With Vaginal Misoprostol for Cervical Ripening in Obese Woman at Term
Active, not recruiting · Not applicable · 1 countries · Registry ID NCT07685756
Active, not recruitingNot applicableInterventional
What this study is about
Cervical ripening balloon compared with vaginal misoprostol for cervical ripening in obese woman at term
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age18 Years to 40 Years
SexFemale
Healthy volunteersNot accepted
ConditionCervical Ripening
Full registry criteria
Inclusion Criteria: * obese women bmi \>30, Bishop score \<6 at time of ripening Singleton pregnancy Gestational age more than 37 weeks Exclusion Criteria: * pregnancy with fetal demise congenital anomalies, History of uterine surgery In active labour \>4 cm dialated Obs complication History of uterine hyper stimulation and uterine rupture Feel malpresentation
Treatments and study arms
Cervical folleys
Device
We will compare effectiveness of cervical ripening with cervical folleys compared to misoprostol in obese women at term
Misoprostol
Drug
We will compare effectiveness of ripening with misoprostol comoared with cervical folleys in obese women at term
Primary outcomes
Less rate of instrumental delivery and c section12 months
Less rate of instrumental delivery and c section in ripening of obese women with cervical folleys as compared to misoprostol at term
Study locations
1 locations were listed when this page was built. The first 40 are shown.
Pakistan institute of medical sciences Islamabad🌐 Islamabad, Punjab Province, Pakistan