to study what effect ambulation has on stages of labor
Not Applicable
- Conditions
- Health Condition 1: O099- Supervision of high risk pregnancy, unspecifiedHealth Condition 2: O099- Supervision of high risk pregnancy, unspecified
- Registration Number
- CTRI/2021/06/034110
- Lead Sponsor
- Government medical college and hospitalChandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All at risk pregnancies >=34 weeks POG with following
Participants will be divided into two groups based on the risk factors that command continuous monitoring or relatively moderate risk permitting intermittent monitoring. Labor will be monitored by either of the two methods:
1.Group A: women who are ambulatory during labor either without electronic monitoring or with intermittent CTG monitoring.
2.Group B: women not ambulating in labor due to continuous CTG monitoring.
Exclusion Criteria
1.Patients on epidural analgesia
2.Patients reporting to labor room in advanced labor. 3.Those who are not willing to participate in labor.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method