Trial Details

Not Recruiting
Basic Information
Clinical ID c2774
Identifier ACTRN12618000507280
Trial Title Bowel preparation assessment using ultrasound examination following standard bowel cleansing regime in patients prior to their colonoscopy.
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions Crohn's;Ulcerative Colitis;Colonoscopy Preparation;Inflammatory Bowel Disease;Bowel Cancer Screening and Surveillance; Crohn's Ulcerative Colitis Colonoscopy Preparation Inflammatory Bowel Disease Bowel Cancer Screening and Surveillance;Inflammatory and Immune System - Other inflammatory or immune system disorders;Oral and Gastrointestinal - Inflammatory bowel disease;Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
Interventions Whether transadbominal ultrasound can accurately assess bowel preparation quality will be determined with observational comparisons with already scheduled colonoscopies and the Boston Bowel Prep Scale and patient reported bowel preparation quality. Both IBD patients and non IBD patients will be included in this study. The transabdominal ultrasound will be performed within 30minutes prior to the scheduled colonoscopy (after they have completed their bowel cleansing). The patients at this point are already in a bed and in hospital gowns and being readied for their colonoscopy. With patient privacy in mind and their curtains closed, only their abdomen will be exposed and the rest covered with the bed sheets, towels and their gown as needed. Then ultrasound Jelly is applied to the abdomen and the ultrasound probes (curved and linear) will be used to obtain ultrasound images of the quality of the bowel prep. Then the jelly is simply wiped off and the patient is ready for their colonoscopy. From previous non-trial ultrasounds for other indications, de-identified images of possible degrees of faeces in the bowel can be used and a numerical scoring system developed (ie from collapsed bowel, to liquid, to semi-solid, to solid/dense material).
Participant Information
Sponsor Concord Hospital Gastroenterology Department
City -
Country/Region Australia
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, ELDER, OLDER_ADULT
Study Design
Study Type Observational
Phase Not Available
Time Information
Start Date 2025-04-24
Primary Completion Date -
Completion Date -