Concentrated beetroot juice
Dietary SupplementNitrate supplementation; natural source of dietary nitrate
Other names: BEET IT sport NITRATE 400 concentrated beetroot shot
NCT Number: NCT05133024
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Antwerp University Hospital, Edegem, Belgium
Postoperative ileus (POI), a transient impairment of gastrointestinal (GI) motility, remains one of the most common complications following abdominal surgery. It is characterized by the presence of nausea and vomiting, the inability to tolerate oral diet, abdominal distension and delayed passage of flatus and stool. POI usually resolves within 3 to 5 days, but when prolonged, it can lead to increased morbidity, prolonged hospitalization and increased healthcare costs. In patients undergoing colorectal surgery, the reported incidence of prolonged POI (PPOI) is 10.2%. Prevention and treatment remains mainly supportive and no single effective treatment is currently available. Because of its multifactorial origin and possible exogenous factors, prevention and treatment generally requires a multimodal approach. Many of these strategies are part of the Enhanced Recovery after Surgery (ERAS) program. The pathophysiology of POI is marked by an acute neurogenic phase followed by a prolonged inflammatory phase and alterations in the enteric neurotransmission. The pathogenesis involves inflammation and oxidative stress, similar to ischemia/reperfusion (I/R) injury. Both I/R injury and POI are associated with downregulation of nitric oxide (NO) synthases. In this sense, beetroot juice holds considerable promise. Beetroot is a rich source of inorganic nitrate. Consumption of nitrate-rich foods increases the concentration of NO metabolites in the blood and tissues via the enterosalivary nitrate-nitrite-NO pathway, independently of the traditional pathway via the endogenous NOS enzymes, which tends to become less effective in older age and in environments wherein oxygen availability is limited such as during hypoxia and I/R injury. Interest goes to the effects of preoperative beetroot juice supplementation on postoperative GI recovery and POI duration after laparoscopic colorectal surgery. A proof of concept study with 12 patients at our lab already showed promising results. We now want to validate the results in a bigger group of patients via a multicentric double-blind randomized controlled prospective phase II study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
General:
Medical:
Surgical:
Nitrate supplementation; natural source of dietary nitrate
Other names: BEET IT sport NITRATE 400 concentrated beetroot shot
Time frame: hours after the end of surgery (suture)
composite endpoint requiring recovery of both upper GI functions (tolerance of a solid diet) and lower GI functions (passage of flatus and stool)
Time frame: first occurence after the end of surgery (suture)
recorded in postoperative days (standard of care) and hours (self-reported in the patient diary)
Time frame: first occurence after the end of surgery (suture)
recorded in postoperative days (standard of care) and hours (self-reported in the patient diary)
Time frame: first occurence after the end of surgery (suture)
liquids: no chewing required, can be quickly swallowed as such, can be ingested with a straw (e.g. water, coffee, tea, juice, soda), recorded in postoperative days (standard of care) and hours (self-reported in the patient diary)
Time frame: first occurence after the end of surgery (suture)
semi-solid food: no or limited biting and chewing required, can be easily swallowed, usually ingested with a spoon or fork (e.g. yoghurt, eggs, soft cheeses), recorded in postoperative days (standard of care) and hours (self-reported in the patient diary)
Time frame: first occurence after the end of surgery (suture)
solid food: proper and sustained biting and chewing required, cannot be swallowed as such, a knife is usually required to cut the food (e.g. steak, raw vegetables, crisp fruit), recorded in postoperative days (standard of care) and hours (self-reported in the patient diary)
Time frame: until hospital discharge after surgery
according to the PPOI definition of Vather et al., 2013
Time frame: until hospital discharge after surgery
from the end of surgery (day 0) until discharge (alive) from hospital, recorded in days (standard of care)
Time frame: until 3 months after surgery
according to Clavien-Dindo, CCI
Time frame: 4 time points: (1) inclusion, (2) day of surgery, (3) postoperative day 1, (4) postoperative day 3
markers for inflammation and oxidative stress, NO bioavailability, intestinal barrier function and permeability
Contact information is provided by the study sponsor or research team.
University Hospital, Ghent
Other
Acronym: BEET IT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07705139
Bowel Sounds, Colonic Diseases
Wuhan, Hubei, China
View Trial DetailsNCT07651722
Neurologic Manifestations, Pain
Tianjin, Tianjin Municipality, China
View Trial DetailsNCT07440667
Brain Diseases, Cardiovascular Diseases
Niğde, Merkez, Turkey (Türkiye)
View Trial DetailsNCT07425249
Delayed Gastrointestinal Motility, Postoperative Gut Dysfunction
Peshawar, KPK, Pakistan
View Trial Details