Trial Information
Inclusion Criteria:
- Colectomy for histologically proven colorectal adenocarcinoma
Exclusion Criteria:
- Pregnancy,
- hereditary cancer,
- history of inflammatory bowel disease,
- metastatic disease at presentation,
- emergency operation,
- major postoperative complications
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care
Outcome Measure:
Assessment of gastrointestinal function-related quality of life at 1, 3 and 6 months postoperatively
Outcome Time Frame:
2 years
Safety Issue:
No
Authority:
Greece: Ethics Committee
Study ID:
SYNBIOTICSCOLON
NCT ID:
NCT01479907
Start Date:
November 2010
Completion Date:
April 2012
Related Keywords:
- Colorectal Neoplasms
- Neoplasms
- Colorectal Neoplasms