IRCT20130812014333N212 IRCT 2023-12-12 Esfahan University of Medical Sciences 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 2023-12-11 anticipated 86 Complete https://irct.ir/trial/73865 interventional Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Randomization using the blocking method with blocks in sizes 6 and 9. For randomization, the site https://www.sealedenvelope.com is used. All codes are recorded on paper and stored in specific envelopes. Each of the generated codes is kept separately inside the envelope and the secretary gives one of these envelopes to the patient before the patient enters the doctor's room. Accordingly, the next patient code is not predictable. The doctor determines which treatments to perform based on the patient's code. Only the physician performing the intervention will be aware of the code assigned to the patient. After evaluating the outcome, based on the patient's name, the collected information will be linked to the assigned code. N/A Colostomy. 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) for the patient, and put him under intravenous nutrition, and the diet does not start earlier than 5 days. Intervention 2: In the second intervention group (ERAS), usually 24 to 48 hours after the operation, depending on when the patient defecates, we start the liquid diet for the patient and do not put the patients under intravenous nutrition. No - There is not a plan to make this available Justification or reason for not sharing IPD is There is no further information