Trial Information
Colonoscopy Screening Using a Novel Slim Colonoscope - a Randomized Controlled Trial
Inclusion Criteria:
- Persons included in the NordICC trial are eligible for inclusion
- For information about the NordICC trial see clinicaltrials.gov NCT00883792
Exclusion Criteria:
- Pregnancy
- Persons younger than 18 years
- Persons unable to comprehend the information given
- not possible to start the examination without prior administration of
sedation/analgesics
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic
Outcome Measure:
Patients´ evaluation of pain and discomfort
Outcome Description:
Analysis of validated feed-back questionnaires to be filled in on the day after the proceudre by the trial participants.
Outcome Time Frame:
24 hours
Safety Issue:
No
Principal Investigator
Michael Bretthauer, MD, Ph.d.
Investigator Role:
Study Chair
Investigator Affiliation:
Oslo University Hospital
Authority:
Norway: Regional Ethics Commitee
Study ID:
PCF-Y0014-L
NCT ID:
NCT01370928
Start Date:
March 2011
Completion Date:
August 2011
Related Keywords:
- Colorectal Cancer
- Adenomas
- Colonoscopy performance
- Pain
- Discomfort
- Screening
- Colorectal cancer
- Colorectal cancer screening, diagnostics of adenomas
- Adenoma
- Colorectal Neoplasms