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Early Feeding vs 5-day Fasting After Distal Elective Bowel Anastomoses in Children. A Randomized Controlled Trial

Not Applicable
Completed
Conditions
Early Feeding
Bowel Anastomosis
Registration Number
NCT01028807
Lead Sponsor
Hospital Infantil de Mexico Federico Gomez
Brief Summary

Purpose:

To determine the safety and efficacy of early enteral feeding after distal (ileum-colon) elective bowel anastomoses in children.

Methods:

Controlled randomized trial including all pediatric patients with distal elective bowel anastomosis, excluding non-elective and high risk patients. VARIABLES:

Demographic characteristics, operative time, anastomosis placement,

Follow up: Tolerability variables: beginning peristalsis, beginning bowel movement, time to full diet intake, post-operative stay. Safety variables: mild and persistent vomiting, persistent abdominal distention, wound infection or dehiscence as well as anastomotic leak or dehiscence, reoperation and death. At the end of surgery were randomized to:

1. Experimental group(EG): Early feeding group, after a 24 hours fasting period, with good abdominal conditions (once the post operative ileus had solved), oral fluids and diet was started.

2. Control group (CG): obligatory 5-day fasting. Once the regular diet was tolerated, the patients were discharged. Statistics: Descriptive statistics for global description. Student's t test for quantitative variables and Chi square test for qualitative variables, a p-value less than 0.05 was considered statistically significant.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • All patients between the ages of 1 month to 18 years old that required elective laparotomy with a distal elective bowel anastomosis (ileum and colon).
Exclusion Criteria
  • Proximal and non elective anastomosis
  • High risk groups:
  • Newborns
  • Upper gastrointestinal tract anastomosis (esophagus, gastric, duodenal or jejunal)
  • Bilious-digestive or rectal anastomosis
  • Immunosuppressed patients
  • Gastrostomy or any pre anastomotic derivation
  • Multiple anastomoses
  • Chronic intestinal obstruction
  • Patients who did not complete the minimum POP follow up of one month.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Need to insert a NGT, beginning peristalsis, beginning bowel movement, time to full diet intake, post-operative stay.First 5 postoperative days
Secondary Outcome Measures
NameTimeMethod
Mild and persistent vomiting, persistent abdominal distention, wound infection or dehiscence as well as anastomotic leak or dehiscence, reoperation and deathFirst 30 postoperative days

Trial Locations

Locations (1)

Hospital Infantil de Mexico

🇲🇽

Mexico Df, DF, Mexico

Hospital Infantil de Mexico
🇲🇽Mexico Df, DF, Mexico

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