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Use of monitoring the pressure in abdominal cavity, in patients undergoing cesarean surgery for baby delivery

Intraabdominal Pressure as a Prognostic Marker in Patients scheduled for Cesarean Section: A Prospective Cohort - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/11/021914
Enrollment
81
Registered
2019-11-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O82- Encounter for cesarean delivery without indication

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

University College of Medical Sciences and GTB Hospital
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
normalization of (intraabdominal pressure) IAP to 12 mmHgTimepoint: At end of surgery—

Secondary

MeasureTime frame
Intraabdominal volume estimated by Abdominal Volume Index; and Abdominal ComplianceTimepoint: Just before and after cesarean delivery—

Countries

India

Contacts

Public ContactSachidananda Das

University College of Medical Sciences and GTB Hospital

drashatyagi@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026