Evaluation of the results of using the ERAS protocol in the process of recovery of children in need ofcolostomy

Not Applicable

Recruiting

• Conditions: Colostomy.; Colostomy complication, unspecified; K94.00

• Registration Number: IRCT20130812014333N212
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

Age between 1 day and 15 years
Patients who are candidates for colostomy surgery
Consent of patients or their parents

Exclusion Criteria

Underlying disease that leads to tissue repair impairments (such as sever malnutrition or connective tissue disease)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Wound infection. Timepoint: One week, 1 month and 2 months after the operation. Method of measurement: doctor's examination.;Re-hospitalization. Timepoint: One week, 1 month and 2 months after the operation. Method of measurement: Asking the patient.