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Creation of a method for seeing harmful effect of saline during and after operation

Development of a Novel Fluid Tolerance index in patients undergoing Emergency Laparotomy - NIl

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/096269
Enrollment
165
Registered
2025-10-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

AIIMS, New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Undergoing emergency abdominal Surgery 2)Duration of surgery at least 2 hours

Exclusion criteria

Exclusion criteria: 1) Refusal to participate 2) CKD Stage IV or V 3) Pregnancy 4) Moribund patients with expected survival less than 48 hours

Design outcomes

Primary

MeasureTime frame
Development of a composite index of cumulative fluid balance, estimated colloidal oncotic pressure, and markers of inflammation/endothelial damage to predict the major post operative complication( Clavein Dindo Grade IV-V)Timepoint: 72 hours

Secondary

MeasureTime frame
Association between Fluid tolerance index and hospital mortalityTimepoint: 72 hours;Association of fluid tolerance index and hospital stayTimepoint: 72 hours;Association between individual components and post operative clinical outcomeTimepoint: 72 hours

Countries

India

Contacts

Public ContactSouvik Maitra

AIIMS , New Delhi

souvikmaitra@live.com8146727891

Outcome results

None listed

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