se of monitoring the pressure in abdominal cavity, in patients undergoing cesarean surgery for baby delivery
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2019/11/021914
- Lead Sponsor
- niversity College of Medical Sciences and GTB Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All pregnant patients with period of gestation of >32 weeks and posted for cesarean section including those with complicated pregnancies will be enrolled.
Exclusion Criteria
Those in labour, with pre-existing organ dysfunction or failure not related to pregnancy, or any contraindication to intravesical pressure measurement such as bladder surgery, haematuria, neurogenic bladder etc.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method normalization of (intraabdominal pressure) IAP to 12 mmHgTimepoint: At end of surgery
- Secondary Outcome Measures
Name Time Method Intraabdominal volume estimated by Abdominal Volume Index; and Abdominal ComplianceTimepoint: Just before and after cesarean delivery