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Clinical Trials/NCT01415817
NCT01415817
Completed
Not Applicable

The Effect of an Intensive Endoscopic Quality Improvement Program (EQUIP) on Improved Detection and Classification of Non-polypoid (Flat and Depressed) and Polypoid Colorectal Adenomas. ("EQUIP" Study)

Mayo Clinic1 site in 1 country15 target enrollmentAugust 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adenomatous Polyps
Sponsor
Mayo Clinic
Enrollment
15
Locations
1
Primary Endpoint
Measurement of overall adenoma detection rate
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Effective colorectal cancer (CRC) screening relies on early identification and removal of both polypoid and non-polypoid lesions with neoplastic potential. The investigators hypothesize that an intensive training program designed to enhance both recognition and classification of lesions with neoplastic potential, will result in an increase in non-polypoid adenoma detection in addition to and independent of an increase in overall adenoma detection rates.

Detailed Description

Our Endoscopic Quality Improvement Program (EQUIP) was a prospective educational intervention with our staff endoscopist as our study population. The investigators measured adenoma detection rates for a baseline period then randomly assigned half of the endoscopists to undergo EQUIP training. The investigators then examined baseline and post-training study adenoma detection rates (ADR's) for all endoscopist (trained and un-trained) to evaluate the impact of training.

Registry
clinicaltrials.gov
Start Date
August 2010
End Date
April 2011
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Colonoscopies performed at Mayo clinic ambulatory surgical center

Exclusion Criteria

  • Procedures for the indication of acute GI hemorrhage
  • Active colitis
  • Hereditary polyposis syndrome
  • Inflammatory bowel disease
  • Incomplete procedures
  • Procedures with surgically altered anatomy (i.e. prior colectomy)
  • Poor bowel preparation (Boston Bowel preparation score \<5) were also excluded.

Outcomes

Primary Outcomes

Measurement of overall adenoma detection rate

Time Frame: 1 year

Primary outcome measures will include overall and per patient adenoma detection rate for polypoid and non polypoid neoplastic lesions.

Secondary Outcomes

  • Measurement of colonoscopy time(1 Year)
  • Endoscopist Acceptance(1 Year)
  • Measurement of total polypectomy rate(1 Year)

Study Sites (1)

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