Clinical Trial: Gastrointestinal Myoelectric Activity Protocol, the G-Tech EEnG Protocol
Study Status: Completed
Recruit Status: Completed
Study Type: Observational
Official Title: A Feasibility Study For Monitoring And Recording Gastrointestinal Myoelectric Activity In Subjects With Suspected Or Diagnosed Irritable Bowel Syndrome (Lbs) And Reports Of GI Pain And Asymptomatic Su
Brief Summary: A feasibility study for monitoring and recording gastrointestinal (GI) myoelectric activity in subjects with suspected or diagnosed irritable bowel syndrome (IBS) and reports of GI pain and asymptomatic subjects without IBS and GI pain.
Detailed Summary: This single-arm, non-randomized feasibility study has been designed to transcutaneously detect and monitor myoelectric intestinal signals temporally associated with the symptoms of patients who report pain and have suspected or diagnosed IBS, and in controls [subjects without suspected IBS or diagnosis of IBS and prior and/or current complaints of pain].
Sponsor: G-Tech Corporation
Current Primary Outcome: Device Success defined as the ability to record myoelectric signals in study subjects. [ Time Frame: Procedure ]
Original Primary Outcome:
Current Secondary Outcome:
Original Secondary Outcome:
Information By: G-Tech Corporation
Dates:
Date Received: September 28, 2012
Date Started: July 2012
Date Completion:
Last Updated: August 11, 2015
Last Verified: August 2015