About this trial
The goal of the BEET IT study is to examine if preoperative intake of beetroot juice can ameliorate gastrointestinal (GI) recovery after colorectal surgery and thereby help to reduce the duration of postoperative ileus (POI) and prevent prolonged POI. Adult patients undergoing laparoscopic colorectal surgery are randomized 1:1 to consume either concentrated beetroot juice (active intervention) or nitrate-depleted concentrated beetroot juice (placebo) during the week before their surgery. Blood, tissue and/or fecal samples are collected at specific time points pre- and/or postoperatively to study markers related to inflammation, oxidative stress and GI function. Patients are followed from the week before surgery (start of the intervention) until 3 months post-surgery. The study takes place at 5 hospitals in Flanders, Belgium.
Eligibility criteria
Qualifiers
Adult patients undergoing elective colonic and upper rectum laparoscopic surgery requiring an anastomosis, without the need of conversion
Disqualifiers
< 18 years of age
Pregnancy or breast feeding
Psychiatric pathology capable of affecting comprehension and judgment faculty
History of inflammatory bowel disease
Trial design
Treatments tested in this trial
- concentrated beetroot juice
Treatment groups
Sponsors and collaborators
University Hospital, Ghent
Lead sponsor
Research Foundation Flanders
Collaborator