patients undergoing lapratomy following trauma will be subjected randomly to ERAS protocol or conventional protocol and their recovery will be assessed

Enhanced recovery after surgery(ERAS) vs. standard care in patients undergoing emergency laparotomy following trauma: a randomised control trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/02/062587

Enrollment

Registered

2024-02-13

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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

Conditions

Health Condition 1: T07- Unspecified multiple injuries

Interventions

Intervention1: Enhanced recovery after surgery protocol: patients undergoing emergency laparotomy following trauma will be subjected to ERAS protocol Control Intervention1: Patients undergoing emergen

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA (American Society of Anesthesiologists) physical status I and II 2. Adequate cognitive capacity

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Length of hospitalizationTimepoint: Length of hospitalization	—

Secondary

Measure	Time frame
2. Time to removal of drainage tubes (nasogastric tube, urinary catheter, abdominal drainage tube)Timepoint: hospitalization;30 days Mortality and readmission ratesTimepoint: 30days postop;Complications (Measured by Clavien-Dindo classification)Timepoint: hospitalization;Need for additional intravenous opiod analgesicsTimepoint: hospitalization;Need for Nasogastric tube insertionTimepoint: hospitalization;Time to first flatus and stoolsTimepoint: hospitalization;Time to resumption of oral feeds (fluids and solid diet)Timepoint: hospitalization	—

Measure

Time frame

2. Time to removal of drainage tubes (nasogastric tube, urinary catheter, abdominal drainage tube)Timepoint: hospitalization;30 days Mortality and readmission ratesTimepoint: 30days postop;Complications (Measured by Clavien-Dindo classification)Timepoint: hospitalization;Need for additional intravenous opiod analgesicsTimepoint: hospitalization;Need for Nasogastric tube insertionTimepoint: hospitalization;Time to first flatus and stoolsTimepoint: hospitalization;Time to resumption of oral feeds (fluids and solid diet)Timepoint: hospitalization

—

Countries

India

Contacts

Public ContactDeepak Sharma

Jawaharlal Institute of Postgraduate Medical Education and Research

drsureshkumar08@yahoo.com8807954780

Outcome results

None listed

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