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Optical Diagnosis Versus Laser Measurement of Polyps' Size During Colonoscopy and Implications for Surveillance

Primary Purpose

Colorectal Polyp

Status
Not yet recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
AccuMeasure
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Colorectal Polyp focused on measuring screening, colonoscopy, surveillance

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • • Adult patients (>18 years)

    • Scheduled for screening, surveillance, or diagnostic colonoscopy
    • Polyps of all forms ≤ 25mm as assessed by the endoscopist

Exclusion Criteria:

  • • Therapeutic colonoscopy;

    • Inflammatory bowel disease (IBD);
    • American Society of Anesthesiologists (ASA) score of >3;
    • Inadequately corrected anticoagulation disorder or anticoagulation medication use;
    • Inability to provide informed consent;
    • Inadequate bowel preparation (Boston bowel preparation scale score [BBPS] <2 per segment);
    • No polyps identified during colonoscopy or only small (<5mm) hyperplastic rectal polyps;
    • Intraprocedural complications, not caused by the study device.

Sites / Locations

  • Radboud university medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Accumeasure last

AccuMeasure first

Arm Description

Optical polyp size assessment, followed by biopsy forceps and then AccuMeasure measurement

optical assessment, followed by AccuMeasure measurement and then biopsy forceps assisted assessment (2)

Outcomes

Primary Outcome Measures

Cohens' Kappa coefficient
interobserver agreement between AccuMeasure and biopsy forceps assisted measurement

Secondary Outcome Measures

Number of Participants with adverse events up to 30 days post colonoscopy
Number of Participants with adverse events
Absolute size differences
Size differences for optical/biopsy forceps/AM assessment as compared to pathology size measurement;
Time for measurement
Time for measurement with AccuMeasure related to number of measurements performed
Endoscopist advised surveillance interval
Endoscopist advised surveillance interval based on optical assessment during colonoscopy, on measurement with an open biopsy forceps, and on measurement with AccuMeasure

Full Information

First Posted
August 3, 2022
Last Updated
January 3, 2023
Sponsor
Radboud University Medical Center
Collaborators
NYU Langone Health, Universitätsklinikum Hamburg-Eppendorf, Indiana University Health, Tel-Aviv Sourasky Medical Center, Bnai Zion Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05489380
Brief Title
Optical Diagnosis Versus Laser Measurement of Polyps' Size During Colonoscopy and Implications for Surveillance
Official Title
Optical Diagnosis Versus Laser Measurement of Polyps' Size During Colonoscopy and Implications for Surveillance (Polyp Size Study)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2023 (Anticipated)
Primary Completion Date
September 1, 2023 (Anticipated)
Study Completion Date
November 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
NYU Langone Health, Universitätsklinikum Hamburg-Eppendorf, Indiana University Health, Tel-Aviv Sourasky Medical Center, Bnai Zion Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Recent updates of the guidelines on polyp surveillance of the American Society of Gastrointestinal Endoscopy (ASGE) and European Society of Gastrointestinal Endoscopy (ESGE) increasingly focus on size of polyps as an important indicator of malignant transformation to colorectal cancer (CRC). However, the interobserver variability in polyp size assessment between optical diagnosis of endoscopists and pathologists is considerable. This may lead to incorrect surveillance intervals in patients at risk for developing colorectal cancer, which may increase the risk of post-colonoscopy CRC (PCCRC). This study aims to assess the precision of a new laser-based measurement system (AccuMeasure, VTM Technologies Ltd.) for polyps during colonoscopy.
Detailed Description
Objective: The main objective is to compare the precision of polyp size measurement by AccuMeasure to biopsy forceps assisted measurement. Secondary objectives are to assess: Time needed for measurement and learning curve, endoscopists advised surveillance intervals based on both measurement methods, and safety. Study design: Multicenter, randomized, parallel group, endoscopist blinded study, including the measurement of 138 polyps during standard colonoscopy. With a polyp detection rate of approximately 40%1, this results in up to 345 patients/colonoscopies to be included. Enrollment will conclude once 138 polyps are included in the study. Study population: All adult patients with screening or surveillance colonoscopies will be asked for informed consent. Polyps smaller than 25mm found during colonoscopy are considered eligible for inclusion. Up to 3 polyps per patient can be included in this study. Intervention: Optical assessment will be performed upon identification of the polyp. Then, measurement with AccuMeasure and biopsy forceps will be performed in a randomized order. The endoscopist will remain blinded to the AccuMeasure measurement outcomes, to avoid a learning effect that could influence subsequent measurements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Polyp
Keywords
screening, colonoscopy, surveillance

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
As optical assessment of polyps has a high interobserver variability, the order of polyps' size measurement using biopsy forceps or AM will be randomized per patient. Therefore, this study consists of two arms: Optical polyp size assessment, followed by biopsy forceps and then AM measurement (1), and optical assessment, followed by AM measurement and then biopsy forceps assisted assessment (2) (Figure 1).
Masking
Outcomes Assessor
Masking Description
the endoscopist will remain blinded to the AccuMeasure measurement outcomes, to avoid a learning effect that could influence subsequent measurements. Even so, all pathologist assessments will be done independent of the study allocation.
Allocation
Randomized
Enrollment
138 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Accumeasure last
Arm Type
Other
Arm Description
Optical polyp size assessment, followed by biopsy forceps and then AccuMeasure measurement
Arm Title
AccuMeasure first
Arm Type
Other
Arm Description
optical assessment, followed by AccuMeasure measurement and then biopsy forceps assisted assessment (2)
Intervention Type
Device
Intervention Name(s)
AccuMeasure
Other Intervention Name(s)
laser-based polyp measurement
Intervention Description
intracolonoscopy measurement of polyps using a laser-based device
Primary Outcome Measure Information:
Title
Cohens' Kappa coefficient
Description
interobserver agreement between AccuMeasure and biopsy forceps assisted measurement
Time Frame
at colonoscopy
Secondary Outcome Measure Information:
Title
Number of Participants with adverse events up to 30 days post colonoscopy
Description
Number of Participants with adverse events
Time Frame
30 days post colonoscopy
Title
Absolute size differences
Description
Size differences for optical/biopsy forceps/AM assessment as compared to pathology size measurement;
Time Frame
at colonoscopy
Title
Time for measurement
Description
Time for measurement with AccuMeasure related to number of measurements performed
Time Frame
at colonoscopy
Title
Endoscopist advised surveillance interval
Description
Endoscopist advised surveillance interval based on optical assessment during colonoscopy, on measurement with an open biopsy forceps, and on measurement with AccuMeasure
Time Frame
At colonoscopy
Other Pre-specified Outcome Measures:
Title
Method of polyp removal
Description
method of polyp removal, i.e., polypectomy, endoscopic mucosal resection, endoscopic submucosal dissection
Time Frame
at colonscopy
Title
BBPS
Description
Boston bowel preparation scale score (BBPS), in which segmental scores of 0 are worst and scores of 3 are best (completely clean)
Time Frame
at colonoscopy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: • Adult patients (>18 years) Scheduled for screening, surveillance, or diagnostic colonoscopy Polyps of all forms ≤ 25mm as assessed by the endoscopist Exclusion Criteria: • Therapeutic colonoscopy; Inflammatory bowel disease (IBD); American Society of Anesthesiologists (ASA) score of >3; Inadequately corrected anticoagulation disorder or anticoagulation medication use; Inability to provide informed consent; Inadequate bowel preparation (Boston bowel preparation scale score [BBPS] <2 per segment); No polyps identified during colonoscopy or only small (<5mm) hyperplastic rectal polyps; Intraprocedural complications, not caused by the study device.
Facility Information:
Facility Name
Radboud university medical center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525GA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The dataset used during this study is available from the corresponding author upon reasonable request
IPD Sharing Time Frame
15y
IPD Sharing Access Criteria
The dataset used during this study is available from the corresponding author upon reasonable request

Learn more about this trial

Optical Diagnosis Versus Laser Measurement of Polyps' Size During Colonoscopy and Implications for Surveillance

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