An observational study to detect the cervical dilatation patterns in low risk pregnant wome
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2023/03/050401
- Lead Sponsor
- Kasturba Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1 Labor with spontaneous and induced onset
2 Gestational age equal to or greater than 37weeks
3 Cervical dilatation <7cm on admission
4 Live singleton
5 Vertex delivery
6 Instrumental vaginal delivery
7 Patients who underwent operative delivery due to causes like failure to progress and fetal distress.
8 Patients who meet the above criteria and had augmentation of labor are also included.
This study will be done on both primigravida and multigravida who satisfy the inclusion criteria.
Exclusion Criteria
1 Patients who had pre-labor rupture of membrane
2 Labor involving epidural analgesia
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method