Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06878378

Risk Factors for Inadequate Bowel Preparation Before Colonoscopy

Led by Changhai Hospital · Updated on 2025-03-18

10000

Participants Needed

1

Research Sites

49 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary objectives of this study are twofold: Firstly, to investigate the current status of bowel preparation protocols and their quality across hospitals at various levels in China, particularly following the release of the updated 2023 bowel preparation guidelines. This aims to standardize and optimize bowel preparation protocols nationwide. Secondly, to identify and analyze risk factors contributing to suboptimal bowel preparation quality in patients undergoing colonoscopy. The study will examine the correlation between these factors and bowel preparation scores, establish a risk prediction model for preparation failure, and provide a theoretical foundation for developing personalized bowel preparation regimens tailored to individual patient characteristics.

CONDITIONS

Official Title

Risk Factors for Inadequate Bowel Preparation Before Colonoscopy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged >18 years scheduled for colonoscopy
  • Written informed consent has been obtained
Not Eligible

You will not qualify if you...

  • History of acute myocardial infarction within 6 months
  • Severe heart, liver, or kidney failure
  • Psychiatric disorders
  • Current use of anticoagulants like aspirin or warfarin
  • Blood clotting disorders
  • Pregnancy or breastfeeding
  • Inflammatory bowel disease or acute intestinal infection within past 2 weeks
  • History of colorectal cancer, familial adenomatous polyposis, or Peutz-Jeghers syndrome
  • History of intestinal obstruction, perforation, stricture, or other conditions preventing colonoscopy completion
  • Not following bowel preparation instructions (e.g., taking less than 80% of prescribed solution)
  • Severe hearing problems, cognitive dysfunction, or inability to cooperate
  • Prior participation in this study with repeat colonoscopy
  • Participation in other clinical trials currently or within past 60 days
  • Refusal to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Changhai Hospital

Shanghai, Shanghai Municipality, China, 200433

Actively Recruiting

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Research Team

Z

Zhao-shen Li

CONTACT

Z

Zi-xuan He

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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