At a glance
ClinicalIndex Comparison RecordN/ACompleted· 136 enrolled
Drug / intervention
G-Tech Gutcheck Myoelectric recording devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Longitudinal Study of Myoelectric GutPrint of Healthy Controls and Crohn's Disease Patients During Flare and Remission
In Brief
An observational study evaluating G-Tech Gutcheck Myoelectric recording device for Crohn Disease. Completed, enrolled 136 participants across 1 site.
Detailed Summary
A feasibility study for assessing and recording myoelectric activity in patients for early detection of flare in patients with Crohn's disease and differentiating the myoelectric signals from Crohn's disease patients in remission state and healthy controls.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsCrohn Disease
CountriesUnited States
Timeline
N/ACompletedFinished
20192020202120222023202420252026
First PostedDec 2018
Enrollment StartJan 2019
Primary CompletionMar 2023
Study CompletionJun 2023
TodayJul 2026
First PostedDec 13, 2018
Enrollment StartJan 1, 2019
Primary CompletionMar 31, 2023
Study CompletionJun 15, 2023
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 7.6 years ago
Interventions
G-Tech Gutcheck Myoelectric recording devicedevice
Three G-Tech patches are placed on the abdomen of the patient to record myoelectric activity.