About this trial
The goal of this study is to assess the clinical and cost-effectiveness of the AI bowel preparation evaluation system in reducing the consumption volume of the standard high-volume PEG regimen before colonoscopy among the older population.
Researchers will compare bowel preparation adequacy and other colonoscopy quality matrices, and patient satisfaction between patients using the AI system and those using Standard Practice.
Eligibility criteria
Qualifiers
individual aged 65 years or above
undergoing colonoscopy for any indication
requiring a standard high-volume PEG regimen for bowel preparation
having a smartphone themselves or their caregivers (including ward nurses) having one will be recruited.
Disqualifiers
allergy to PEG,
suspected or diagnosed gastrointestinal obstruction or perforation,
suspected or diagnosed ileus
suspected or diagnosed gastric retention
Trial design
Treatments tested in this trial
- AI