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The application of nutrition meal replacement based on the ERAS concept in the bowel preparation of colonoscopy: a multicenter randomized controlled trial

The application of nutrition meal replacement based on the ERAS concept in the bowel preparation for patients undergoing colonoscopy/surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091844
Enrollment
Unknown
Registered
2024-11-05
Start date
2024-11-15
Completion date
Unknown
Last updated
2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Early colorectal cancer

Interventions

Intervention group(nutrition meal replacement group):Subjects had a low-residue meal prepared by themselves for breakfast the day before the examination. The nutritional supplement powder was used for
Control group(traditional diet group):The patients were given a list of low-residue diet options. Patients should consume their own prepared low-residue diet for breakfast, lunch and dinner the day be

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1)Patients who are undergoing colonoscopy for the first time without any dietary restrictions; (2)Ages ranging from 18 to 80 years old; (3) Those who have signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Pregnant or breastfeeding women; (2) Severe heart, kidney, lung, or liver diseases; (3)Severe electrolyte disorders; (4)Intestinal obstruction, toxic megacolon, severe inflammatory bowel disease; (5)Severe gastrointestinal bleeding (Hb < 70g/L); (6) Those with a history of major abdominal surgery that could easily lead to intestinal adhesions (such as colectomy for colon cancer, liver transplantation, pancreatic surgery); (7)Those with identified colon polyps, adenomas, or other lesions who are undergoing colonoscopy for treatment purposes; (8)Those who refuse to use polyethylene glycol electrolyte solution for bowel cleansing; (9)Those who cannot undergo body composition testing; (10) Those who are related to this clinical trial study.

Design outcomes

Primary

MeasureTime frame
Boston bowel preparation score;Bubble score;colonoscopy insertion time;qualified rate of bowel preparation;

Secondary

MeasureTime frame
tumor detection rate;starving and thirsty level;

Countries

China

Contacts

Public ContactWen Hu; Lei Shi

West China Hospital of Sichuan University

wendy_nutrition@163.com+86 189 8060 1164

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026