Trial Details

Recruiting
Basic Information
Clinical ID c5423
Identifier ACTRN12623001315606
Trial Title Do perioperative synbiotics reduce postoperative infectious complications in patients undergoing elective colorectal resection?
Trial URL Visit Original Page
Study Information
Study Results

NULL
Conditions Colorectal disease;Postoperative infection;Colorectal cancer;Inflammatory bowel disease; Colorectal disease Postoperative infection Colorectal cancer Inflammatory bowel disease;Surgery - Other surgery;Infection - Studies of infection and i
Interventions The intervention is a synbiotic powder manufactured by the Sydney based company ProGood. Synbiotics are a combination of probiotics and prebiotics. Probiotics and synbiotics are classified as food supplements, not medicines. The selected synbiotic
Participant Information
Sponsor The University of Auckland
City NULL
Country/Region New Zealand
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, ELDER, OLDER_ADULT
Study Design
Study Type Interventional
Phase NULL
Time Information
Start Date NULL
Primary Completion Date NULL
Completion Date NULL