A multicentre randomised controlled trial of the modified Kono S anastomosis versus the stapled side to side anastomosis after ileocolic resection for Crohn’s disease
Not Applicable
Recruiting
- Conditions
- Crohn's diseaseileocolic resectionOral and Gastrointestinal - Crohn's diseaseSurgery - Other surgery
- Registration Number
- ACTRN12622000809730
- Lead Sponsor
- Royal Brisbane Brisbane & Women's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 65
Inclusion Criteria
Adults, 18 years and over.
Crohn’s disease as diagnosed in accordance with the Lennard-Jones criteria.
First or second ileocolic resection.
Willingness to comply with study requirements and follow up.
Surgery to be performed within 30 days of randomization.
Provide written informed consent.
Exclusion Criteria
Emergency surgery where randomisation or informed consent is not possible.
Two or more prior ileocolic resections.
Oral Steroids at 20mg prednisone or over for 4 weeks or equivalent, prior to surgery.
Any patient whose medical condition requires a stoma.
Pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method