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NCT01952418 Clinical Trial

Effect of Video Monitor Size on Adenoma Detection Rate

Colon Adenoma Clinical Trial

Official title:
Effect of Video Monitor Size on Adenoma Detection Rate

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01952418
Other study ID # 2013p001462
Secondary ID
Status Recruiting
Phase N/A
First received September 19, 2013
Last updated September 16, 2014
Start date October 2013
Est. completion date June 2015

Study information
Verified date September 2014
Source Massachusetts General Hospital
Contact Norman S Nishioka, MD
Phone 617-726-4422
Email nnishioka@partners.org
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The goal of this study is to compare the adenoma detection rate achieved while using either a 24" video monitor or a 32" video monitor.

Recruitment information / eligibility
Status Recruiting
Enrollment 20
Est. completion date June 2015
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 80 Years
Eligibility Inclusion Criteria:

- Physician endoscopist performing colonoscopy at Massachusetts General Hospital GI Endoscopy Unit

Exclusion Criteria:

- Refusal to participate

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intervention

Device:
• Monitor size
Subjects will be randomized to perform their colonoscopy procedures while viewing a large (32") video monitor or the standard (24") video monitor.

Locations
Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)
Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Adenoma detection rate 1 week No
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