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NCT Number: NCT05133024

Use of Beetroot Juice to Protect Against Postoperative Ileus Following Colorectal Surgery: BEET IT Study

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Antwerp University Hospital, Edegem, Belgium

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients undergoing elective colonic and upper rectum laparoscopic surgery requiring an anastomosis, without the need of conversion

Exclusion criteria

General:

  • < 18 years of age
  • Pregnancy or breast feeding

Medical:

  • Psychiatric pathology capable of affecting comprehension and judgment faculty
  • History of inflammatory bowel disease
  • Chronic vascular disease affecting the intestines
  • Chronic constipation (<= 2 bowel movements/week)
  • Previous abdominal or pelvic radiation treatment
  • Recent (< 3 months before inclusion) or current intra-abdominal infection or inflammation (e.g. diverticulitis, appendicitis, cholecystitis)
  • Use of gut motility influencing agents (e.g. tricyclic antidepressants, chronic use of laxatives)
  • Use of nitrates (e.g. isosorbide dinitrate, nitroglycerin), including daily consumption of beetroot juice (unless stopped for a month prior to the intervention period)
  • Hypotension (< 100/60 mmHg)
  • Uncontrolled diabetes mellitus
  • Renal or hepatic insufficiency
  • Known allergies or intolerances to beetroot, nitrates/nitrites
  • Enrollment in other clinical trials/experiments, unless approved by the Ethics Committee(s)

Surgical:

  • History of prior colorectal surgery
  • Emergency surgery
  • Open surgery
  • Colorectal surgery not requiring an anastomosis (e.g. colotomy, wedge resection)
  • More than 1 bowel anastomosis planned
  • Concomitant surgical procedures required (e.g. resection of liver or lung metastases)
  • Protective stoma planned

Treatment and study plan

Concentrated beetroot juice

Dietary Supplement

Nitrate supplementation; natural source of dietary nitrate

Other names: BEET IT sport NITRATE 400 concentrated beetroot shot

Primary outcomes

  1. Postoperative recovery of gastrointestinal (GI) function

    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)

Secondary outcomes

  1. First passage of flatus

    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)

  2. First passage of 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)

  3. First tolerance of liquids

    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)

  4. First tolerance of a semi-solid diet

    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)

  5. First tolerance of a solid diet

    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)

  6. Incidence and recovery of PPOI

    Time frame: until hospital discharge after surgery

    according to the PPOI definition of Vather et al., 2013

  7. Postoperative length of hospital stay

    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)

  8. Number and types of postoperative complications

    Time frame: until 3 months after surgery

    according to Clavien-Dindo, CCI

  9. Levels of specific biomarkers in blood, tissues and/or feces

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Karen De Meuleneir, MSc

CONTACT

[email protected]

Wim Ceelen, MD, PhD

CONTACT

[email protected]

093326251 ext. +32

Sponsors and collaborators

Lead sponsor

University Hospital, Ghent

Other

Collaborators

  • Research Foundation Flanders

Registry information

Acronym: BEET IT

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Nov 24, 2021
Registry last updated
Feb 10, 2026

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.

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