Comparison hospital outcome of early oral feeding and late oral feeding in elective intestinal anastomosis in surgical cases
Not Applicable
- Conditions
- eed for intestinal anastomosis.
- Registration Number
- IRCT201108067238N1
- Lead Sponsor
- Tanriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Inclusion critera: intestinal anastomosis in elective surgical patients; no associated surgical or medical disease; patient's consent to the study; no associated malnutrition
Exclusion criteria: age over 75 years or less than 15 years of age; associated malnutrition; severe associated diseases; emergent cases, intestinal obstruction or peritonitis
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Distension. Timepoint: First to fifth post-operative days. Method of measurement: History & Physical Examination.
- Secondary Outcome Measures
Name Time Method Abdominal pain. Timepoint: First to fifth post-operative days. Method of measurement: History.;Vomitting & nausea. Timepoint: First to fifth post-operative days. Method of measurement: History.;Duration of admission. Timepoint: Days in hospital. Method of measurement: Counting days.;Early complications. Timepoint: First to fifth post-operative days. Method of measurement: History, physical examination and diagnostic techniques.