Does Inspection of Colonic Mucosa During Insertion Improve Adenoma Detection?

Overview

This is a prospective randomised controlled trial to assess an intervention of inspection during both phases of colonoscopic examination ( insertion and withdrawal) improve adenoma detection rate when compared to inspection only during withdrawal.

Full Title of Study: “Does Careful Inspection of Colonic Mucosa During Insertion and Withdrawal During Bowel Scope Improve Rate of Adenoma Detection?”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Diagnostic
    • Masking: None (Open Label)
  • Study Primary Completion Date: August 30, 2018

Detailed Description

Successful implementation of colorectal screening programmes and improvement in colonoscopic technology have resulted in significant decrease in colorectal cancer incidence and mortality. Effectiveness of colonoscopy largely depends on detection and removal of adenomas before they become cancerous. Despite the vast improvement in colonoscopy training and technology, it remains as an imperfect tool. It has been reported that the adenoma miss rate during colonoscopy varies between 6-27% in clinical practice. Adenoma Detection Rate (ADR) is a surrogate marker of efficient colonoscopy. Researchers continue to explore various methods and technologies to improve adenoma detection such as frequent position changes, routine use of antispasmodics and devices to improve the mucosal visibility (third eye retro view scope, Transparent cap, Endocuff). However, all the techniques are focused on the withdrawal stage of the examination. Colonic examination is traditionally performed with rapid passage of colonoscope to the caecum and a careful examination of mucosa is carried out during the withdrawal phase. Polyps are removed during the withdrawal phase. It is well known from expert opinion that some polyps are detected during the insertion phase rather than withdrawal phase especially in sigmoid and transverse colon. This could be due to different anatomical configuration of colon during insertion and withdrawal. During insertion phase colonic mucosa is stretched and the folds are splayed due to the formation of loops and angulation hence affects the visualised area of the mucosa ahead of the colonoscope. During withdrawal, the colon is shortened and the adjacent folds are brought closer to each other. On withdrawal colon is much straighter. Therefore, it may expose different portions of colonic mucosal surface on insertion and withdrawal. Flexible sigmoidoscopy Bowel cancer screening programme (Bowel Scope) has been successfully implemented since May 2013. Initial reports suggest ADR within Bowel Scope screening varies considerably. Therefore, we propose a simple technique to improve ADR in Bowel Scope Screening. RATIONALE FOR CURRENT STUDY Recent report suggests that ADR within Bowel Scope screening (BSS) varies considerably. We propose a small technical alteration to improve ADR in BSS. A recent prospective trial highlighted that if polypectomy was performed only during Withdrawal Phase (WP) when compared to performing careful inspection and polypectomy during Inspection Phase (IP) plus WP, polyps could be missed in about 7% of patients. We hypothesised that careful inspection and polypectomy during both phases would be complementary and it would increase ADR by complete visualisation of recto sigmoid mucosa during Bowel Scope.

Interventions

  • Other: Colonic inspection
    • Participants who are randomised to undergo the intervention will have the colonic mucosa examined during inspection and withdrawal phase of examination

Arms, Groups and Cohorts

  • Placebo Comparator: Inspection on withdrawal
    • Participants colonic mucosa will be examined only during withdrawal phase of the examination.
  • Active Comparator: Inspection on insertion and withdrawal
    • Participants colonic mucosa will be examined during insertion and withdrawal phase of the examination

Clinical Trial Outcome Measures

Primary Measures

  • Adenoma detection rate
    • Time Frame: 8 months
    • Number of participants with at least one adenoma

Secondary Measures

  • Polyp detection rate
    • Time Frame: 8 months
    • Number of patients with at least one polyp
  • Mean number of adenoma per patient
    • Time Frame: 8 months
    • Number of adenomas divided by the number of patients in that group
  • Total procedure time
    • Time Frame: 8 months
    • Time taken to complete the procedure
  • Advanced adenoma detection rate
    • Time Frame: 8 months
    • Number of patients with adenoma larger than 10mm and or consists of villous histology or high grade dysplasia

Participating in This Clinical Trial

Inclusion Criteria

  • Participants who are referred for a bowel scope screening procedure Exclusion Criteria:

  • Patients lacking capacity to give informed consent – Pregnant women – Age less than 55 years – Uncorrectable coagulopathy – Patients who are not fit for flexible sigmoidoscopy – Incomplete procedure

Gender Eligibility: All

Minimum Age: 55 Years

Maximum Age: 79 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • London North West Healthcare NHS Trust
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Rajaratnam Rameshshanker, MBBS,MRCP, Principal Investigator, London North West Healthcare NHS Trust

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.