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NCT07608120Recruiting

Electrolyte Beverage Combined With Polyethylene Glycol for Colonoscopy Bowel Preparation

Randomized Controlled Trial of Different Ratios of Electrolyte Beverage and Water Combined With Polyethylene Glycol on Bowel Preparation Quality and Ingestion Rhythm Before Colonoscopy

Source: ClinicalTrials.gov · Last updated 27 May 2026

Brief summary (registry, in English)

This randomized controlled trial aims to evaluate the effects of different ratios of electrolyte beverage and water combined with polyethylene glycol (PEG) on bowel preparation quality before colonoscopy. Participants undergoing elective colonoscopy will be randomly assigned to one of three bowel preparation regimens: PEG prepared with water only, PEG prepared with a low ratio of electrolyte beverage and water, or PEG prepared with a medium ratio of electrolyte beverage and water. The primary outcome is adequate bowel preparation assessed by the Boston Bowel Preparation Scale (BBPS). Secondary outcomes include bowel preparation completion rate, tolerability, adverse events, repeat colonoscopy rate, adenoma detection rate, and ingestion rhythm characteristics during bowel preparation. This study also aims to explore whether electrolyte beverage-assisted bowel preparation may improve bowel cleansing quality by influencing participants' ingestion rhythm and adherence during PEG intake.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
405 (estimated)
First submitted
18 May 2026
Start date
18 May 2026
Primary completion date
31 Jan 2027
Lead sponsor
Nanfang Hospital, Southern Medical University
NCT number
NCT07608120

What you commit to

  • Study type: Interventional
  • Planned participants: 405
  • From 18 May 2026 to the primary completion date, 31 Jan 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously diagnosed colorectal cancer, intestinal obstruction, or suspected intestinal obstruction;

Other illness

  • Active gastrointestinal bleeding or a definite history of gastrointestinal bleeding within the past 4 weeks (including melena, hematochezia, or hematemesis);
  • Severe renal insufficiency, decompensated heart failure, significant electrolyte imbalance, or other conditions unsuitable for PEG bowel preparation;
  • Known allergy to polyethylene glycol or components of the electrolyte beverage used in the study;
  • Any other condition considered by the investigators to make the participant unsuitable for the study.

Other

  • Pregnant or breastfeeding women;

Who the study is looking for

  • Adults aged 18-75 years scheduled to undergo elective colonoscopy
  • Meet the standard clinical indications for colonoscopy;
  • Able to understand and comply with the bowel preparation procedure and complete oral polyethylene glycol (PEG) intake as required;
  • Able to comply with study-related data collection and follow-up;
  • Provide written informed consent voluntarily.

Age in the registry: 18 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nanfang Hospital, Southern Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.