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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04749303
Other study ID # 2020.327
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date August 31, 2021

Study information

Verified date February 2021
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess whether the use of large screen during colonoscopy will increase adenoma detection rate.


Description:

Colorectal cancer is the 3rd most common cancer in the world. Recently in Hong Kong it has surpassed lung cancer to be the most common cancer. Hence it is essential not only to have up-to-date surgical and oncological treatment but also a need an effective preventative strategy. In the past few decades, removal of pre-malignant colonic lesions such as adenomas have been shown to prevent development of colorectal cancers. Colonoscopy is currently the only technique which can perform both detection and treatment during the same procedure. However, concerns have been raised about the effectiveness of colonoscopy in the prevention of CRC after several studies reported unexpected high incidence rates of interval carcinomas (IC), especially in the proximal colon. Most ICs are suspected to arise from missed colon lesions during colonoscopy. Factors concerning missed colonic lesions are multifactorial such as adequate bowel preparation, skill level of endoscopists, the number of endoscopy staff in the room as "eyes" to help with polyp detection and withdrawal time. Following a pilot study in our endoscopy unit, we believe the size of the screen projecting the endoscopic image may have a positive influence on adenoma detection. Therefore, we feel that a well-designed and adequately powered randomised controlled trial may help to confirm this.


Recruitment information / eligibility

Status Recruiting
Enrollment 656
Est. completion date August 31, 2021
Est. primary completion date June 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Patients aged 18 years or above - Referred to the endoscopy unit for diagnostic or surveillance colonoscopy Exclusion Criteria: - Familial history of Familial adenomatous polyposis or Hereditary non-polyposis colorectal cancer - Known history of inflammatory bowel disease - Emergency endoscopy of any nature (such as for gastrointestinal bleeding, assessment of large bowel investigation and colonic decompression) - Patients with colostomy - Previously incomplete colonoscopy (not including insufficient preparation) - Patients with known palliative colorectal malignant disease Patients with coagulopathies Inability to give informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Large Screen
Large screen size is 4x larger than standard screen, we hope that the colonoscopies carried out with large screens will confer to better lesion detection

Locations

Country Name City State
Hong Kong Prince of Wales Hospital Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adenoma Detection Rate (ADR) ADR is defined as the proportion of an endoscopist's screening colonoscopies in which one or more adenomas have been detected in patients 12 months
Secondary Mean number of adenomas detected per colonoscopy Mean number of adenomas detected per colonoscopy found in each arm 12 months
Secondary Mean number of sessile serrated polyps Mean number of sessile serrated polyps found in each arm 12 months
Secondary Caecal intubation rate percentage of caecal intubation rate in each arm 12 months
Secondary Bowel cleansing level According to the Boston bowel preparation scale (0=worst bowel preparation to 9= best bowel preparation). Comparison of each arm. 12 months
Secondary Procedure Time Both intubation and withdrawal time will be recorded. Comparison of each arm. 12 months
Secondary Severe adverse events SAEs of both arms for comparisons 12 months
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