To study the effect on cesarean section rate by monitoring the labor progression with the use of 2 different partographs
Not Applicable
Completed
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2021/10/037302
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 570
Inclusion Criteria
All pregnant women (both primigravida and multigravida) with singleton pregnancy at >36 weeks gestation admitted for vaginal delivery.
Exclusion Criteria
1.Women admitted for elective LSCS.
2.Women with multifetal pregnancy.
3.Women with malpresentation.
4.Women with h/o uterine surgery eg: cesarean section, myomectomy etc.
5.Women with contracted pelvis or cephalopelvic disproportion.
6.Patients not giving consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method