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Enhanced Recovery After Surgery (ERAS) in Patients Undergoing Emergency Laparotomy

NCT06182488 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2023-12-27

No results posted yet for this study

Summary

The goal of this clinical trial is to test the safety and effectiveness of the ERAS protocols compared to a conventional care protocols in patients who received emergency laparotomy. The main question it aims to answer are:

• Can the ERAS protocols be used safely and effectively in patients undergoing emergency laparotomy? Participants will be randomised into the ERAS group and the conventional group and will be given the ERAS protocols and the conventional protocols in the perioperative period.

Researchers will compare the ERAS group with the conventional group to see if the ERAS programme is effective.

Conditions

  • Acute Abdomen
  • Abdominal Trauma
  • Emergency Surgery

Interventions

OTHER

ERAS protocols

ERAS protocols for emergency abdominal surgery

OTHER

Conventional protocols

Conventional protocols for emergency abdominal surgery

Sponsors & Collaborators

  • Tianjin Hospital

    collaborator OTHER

  • Tianjin Medical University

    lead OTHER

Principal Investigators

  • Hong Zheng, MD · Tianjin First Central Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-01
Primary Completion
2023-11-30
Completion
2024-05-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06182488 on ClinicalTrials.gov