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

Evaluation of the results of using the ERAS protocol in the process of recovery of children in need ofcolostomy reversal referred to Isfahan

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130812014333N212
Enrollment
86
Registered
2023-12-12
Start date
2023-12-11
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Colostomy. Colostomy complication, unspecified

Interventions

Intervention 1: In the first intervention group (traditional protocol), the patient remains fasting for 5 days after the operation, and we prescribe albumin, vitamins and carbohydrates (dextrose serum

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 15 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mehrdad Hosseinpour

Esfahan University of Medical Sciences

Meh_hosseinpour@yahoo.com+98 31 3792 3071

Outcome results

None listed

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