Comparison Between HD+ Endoscopy and Standard Videoendoscopy in Screening Colonoscopy

Sponsor
Johannes Gutenberg University Mainz (Other)
Overall Status
Unknown status
CT.gov ID
NCT00792649
Collaborator
(none)
200

Study Details

Study Description

Brief Summary

Colonoscopy is the accepted gold standard for screening of colorectal cancer. However, small and flat neoplastic lesions might be overlooked with standard video endoscopes. The new available EPKi system (Pentax, Japan) enables with HD+ imaging resolution above HDTV standard. Aim of the study was to test the efficacy of HD+ colonoscopy alone and in conjunction with I-Scan (newly developed post processing digital filter)in comparison to standard videoendoscopy

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Study Start Date :
    Feb 1, 2008

    Arms and Interventions

    Arm Intervention/Treatment
    1

    screening colonoscopy with HD+ endoscopes

    2

    screening colonoscopy with standardvideoendoscopes

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • Consecutive patients scheduled for screening colonoscopy
      Exclusion Criteria:
      • Inflammatory bowel disease

      • Cancer

      • Pregnancy

      • Inability to obtain informed consent

      • Prothrombin time < 50% of control

      • Partial thromboplastin time > 50 seconds

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • Johannes Gutenberg University Mainz

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00792649
      Other Study ID Numbers:
      • 837.386.07
      First Posted:
      Nov 18, 2008
      Last Update Posted:
      Nov 18, 2008
      Last Verified:
      Feb 1, 2008
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Nov 18, 2008