Comparison of Foleys catheter with PGE2 and foleys catheter with misoprostol as a induction method for preterm fetuses
Not yet recruiting
- Conditions
- Sequelae of complication of pregnancy, childbirth, and the puerperium,
- Registration Number
- CTRI/2023/06/054373
- Lead Sponsor
- Annie Jesline Dmello
- Brief Summary
This study aims to determine the effectiveness of intracervical foleys catheter with extra amniotic saline infusion (EASI) versus intracervical foleys with misoprostol for cervical ripening in extremely, moderate and very preterm fetuses.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Female
- Target Recruitment
- 56
Inclusion Criteria
All pregnant females between gestational age of 26 weeks to 34 weeks requiring termination of pregnancy due to Intra uterine fetal demise, severe oligohydramnios, lethal congenital abnormality.
Exclusion Criteria
presence of cervicovaginal infection, multiple pregnancy, antepartum hemorrhage, placenta previa.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method change/ improvement in bishops score 8th hourly reassessment
- Secondary Outcome Measures
Name Time Method mode of delivery postpartum sepsis rate
Trial Locations
- Locations (1)
Karnataka Institute Of Medical Sciences and Research Hospital
🇮🇳Dharwad, KARNATAKA, India
Karnataka Institute Of Medical Sciences and Research Hospital🇮🇳Dharwad, KARNATAKA, IndiaAnnie Jesline DmelloPrincipal investigator8310508268a96jesline@gmail.com