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Comparison of Newer Colonoscopy Devices With Standard Forward Viewing (SFV) Colonoscopes in Daily Practice

Primary Purpose

Adenoma Detection Rate

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
difference between colonoscopes
Sponsored by
Gastroenterologie Baden-Wettingen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Adenoma Detection Rate

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • all patient fit for ambulatory colonoscopy

Exclusion Criteria:

  • for Endocuff stricturing divertculosis

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Other

    Other

    Other

    Arm Label

    FUSE

    HD Pentax i10 colonoscopes

    Endocuff

    Arm Description

    wide angle colonoscope

    SFV instrument

    Cuff on SFV

    Outcomes

    Primary Outcome Measures

    Adenoma detection rate
    adenoma counts

    Secondary Outcome Measures

    time for endoscopy (time to ileum, withdrawal and intervention time). Medication, Satisfaction on VAS
    different endoscopy characteristics

    Full Information

    First Posted
    July 11, 2020
    Last Updated
    February 8, 2021
    Sponsor
    Gastroenterologie Baden-Wettingen
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04472741
    Brief Title
    Comparison of Newer Colonoscopy Devices With Standard Forward Viewing (SFV) Colonoscopes in Daily Practice
    Official Title
    Comparison of Newer Colonoscopy Devices With Standard Forward Viewing (SFV) High Definition Colonoscopes in Daily Practice
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2021
    Overall Recruitment Status
    Completed
    Study Start Date
    March 1, 2015 (Actual)
    Primary Completion Date
    September 25, 2019 (Actual)
    Study Completion Date
    September 25, 2019 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Gastroenterologie Baden-Wettingen

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Retrospective data analysis of comparsion of 3 types of colonoscopes in daily practice (FUSE Full spectrum colonoscopy with 330° angle of view vs Pentax standard HD-colonoscopes and Pentax plus Endocuff): medical device of the category IIb (CE-marked device used within its intended purpose)
    Detailed Description
    From March 2015 through February 2017 (phase A) patients referred for ambulant colonoscopy in a private Swiss gastroenterologist's practice were alternatingly allocated to one of the two endoscopy theatres. One equipped with a FUSE® endoscopy system from Endochoice (later: Boston Scientific, nA/FUSE®=1044 examinations), the other with an EPKi Processor and Pentax i10 colonoscopes (nA/Pentax=934 examinations). In March 2017 a second doctor joined the practice, but did not contribute to the study. These organizational changes required randomization to be switched from per-patient alternation to per-day alternation in phase B from March 2018 through September 2019. In phase B the FUSE® system was unchanged (nB/FUSE®=1386 examinations), while the Pentax i10 colonoscopes were additionally equipped with Endocuff® (nB/Endocuff®=750 examinations). Patients with contraindica-tion against Endocuff® (known or found diverticular stenosis) were excluded from the study (nB/removed=127). Patients were given their appointments to any free slot throughout the week without stratification. The study and data analysis was consented by the ethical committee EKNZ Ethikkom-mission Nordwest- und Zentralschweiz (Project-ID 2019-01643). All procedures were performed by one experienced endoscopist (board certified 2004) under nurse assisted propofol sedation (NAPS). Baseline characteristics, age, sex, BMI, smoking habits, diabetes as well as quality of bowel prepara-tion (measured by BBPS score) and indication for colonoscopy (screening, surveillance, diagnostic, such as diarrhea, bleeding, persistent abdominal pain) were assessed. Amount of sedatives, other medications given during endoscopy (e.g. Buscopan®) and time for the endoscopy e.g. time to ile-um, retraction time (pullback time minus intervention time) and time for intervention were measured by the assistant with a stopwatch. These parameters, polyp counts, size and their localisation (entered in a table and to an anatomical scheme), and satisfaction for all parts of the examination (bowel prep and overall satisfaction) were realtime entered to the database by a tablet computer. The data entry was done coded. Only the main investigator could subdue each single patient. Statistics were done with a professional statistics, the co-author Dr. Leiner

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Adenoma Detection Rate

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    4114 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    FUSE
    Arm Type
    Other
    Arm Description
    wide angle colonoscope
    Arm Title
    HD Pentax i10 colonoscopes
    Arm Type
    Other
    Arm Description
    SFV instrument
    Arm Title
    Endocuff
    Arm Type
    Other
    Arm Description
    Cuff on SFV
    Intervention Type
    Device
    Intervention Name(s)
    difference between colonoscopes
    Intervention Description
    patients have been randomly assigned for colonoscopy with FUSE or HD SFV endoscopes with or without Endocuff
    Primary Outcome Measure Information:
    Title
    Adenoma detection rate
    Description
    adenoma counts
    Time Frame
    within 45 minutes of examination
    Secondary Outcome Measure Information:
    Title
    time for endoscopy (time to ileum, withdrawal and intervention time). Medication, Satisfaction on VAS
    Description
    different endoscopy characteristics
    Time Frame
    within 45 minutes of examination

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: all patient fit for ambulatory colonoscopy Exclusion Criteria: for Endocuff stricturing divertculosis

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Comparison of Newer Colonoscopy Devices With Standard Forward Viewing (SFV) Colonoscopes in Daily Practice

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