A clinical trial to compare the concurrent use of vaginal misoprostol and transcervical foley catheter inflated with 60 ml vs 80 mlin nulliparous women at term for induction of labor
Not Applicable
Completed
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2021/09/036921
- Lead Sponsor
- Dr RPGMC Kangra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
Single live intrauterine fetus with cephalic presentation
period of gestationgreater than equal to 40 weeks
Exclusion Criteria
women in spontaneous labor
fetal malpresentation
rupture of membranes
previous uterine surgery
multifetal gestation
antepartum haemorrhage
all contraindications to vaginal delivery(rachitic elvis, carcinoma cervix,CPD)
Intruterine fetal death
allergy to latex
placenta vasa previa or cord presentation
active genital herpes
contraindications to prostaglandins
any co morbid surgical illness
Non reassuring fetal heart rate
any previous attempt of IOLin present pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method