INWARD: Does Inspection of Colonic Mucosa During Insertion Improve Adenoma Detection?

Sponsor
London North West Healthcare NHS Trust (Other)
Overall Status
Completed
CT.gov ID
NCT03254030
Collaborator
(none)
490
1
2
21.2
23.2

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Colonic inspection
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
490 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants are randomised to undergo the flexible sigmoidoscopy screening examination either for control or intervention group. Control group is to undergo inspection of colonic mucosa only during withdrawal phase of the examination. Intervention group will undergo the examination during which the colonic mucosa will be inspected during inspection and withdrawal phase.Participants are randomised to undergo the flexible sigmoidoscopy screening examination either for control or intervention group. Control group is to undergo inspection of colonic mucosa only during withdrawal phase of the examination. Intervention group will undergo the examination during which the colonic mucosa will be inspected during inspection and withdrawal phase.
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Does Careful Inspection of Colonic Mucosa During Insertion and Withdrawal During Bowel Scope Improve Rate of Adenoma Detection?
Actual Study Start Date :
Mar 27, 2017
Actual Primary Completion Date :
Aug 30, 2018
Actual Study Completion Date :
Dec 31, 2018

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Inspection on withdrawal

Participants colonic mucosa will be examined only during withdrawal phase of the examination.

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

    Participants colonic mucosa will be examined during insertion and withdrawal phase of the examination

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

    Primary Outcome Measures

    1. Adenoma detection rate [8 months]

      Number of participants with at least one adenoma

    Secondary Outcome Measures

    1. Polyp detection rate [8 months]

      Number of patients with at least one polyp

    2. Mean number of adenoma per patient [8 months]

      Number of adenomas divided by the number of patients in that group

    3. Total procedure time [8 months]

      Time taken to complete the procedure

    4. Advanced adenoma detection rate [8 months]

      Number of patients with adenoma larger than 10mm and or consists of villous histology or high grade dysplasia

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    55 Years to 79 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 NorthWest London Hospitals - NOrthwick park hospital Harrow Middlesex United Kingdom HA1 3UJ

    Sponsors and Collaborators

    • London North West Healthcare NHS Trust

    Investigators

    • Principal Investigator: Rajaratnam Rameshshanker, MBBS,MRCP, London North West Healthcare NHS Trust

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    London North West Healthcare NHS Trust
    ClinicalTrials.gov Identifier:
    NCT03254030
    Other Study ID Numbers:
    • RD16/117
    First Posted:
    Aug 18, 2017
    Last Update Posted:
    Sep 10, 2020
    Last Verified:
    Sep 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by London North West Healthcare NHS Trust
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 10, 2020