CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 32 enrolled
Drug / intervention
mucosal impedance (MI) testingother
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.

Search/NCT03165058
NCT03165058N/ACompleted

Assessment of Colonic Epithelial Integrity With Mucosal Impedance

Vanderbilt University Medical Center·observational·Posted May 24, 2017·Updated May 7, 2021

In Brief

An observational study evaluating mucosal impedance (MI) testing for Inflammatory Bowel Diseases. Completed, enrolled 32 participants across 1 site.

Detailed Summary

In this study, the investigators propose to use mucosal impedance (MI), a minimally invasive technology, to detect mucosal damage (i.e. barrier dysfunction) based on mucosal conductivity changes in the colonic epithelium.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedMay 24, 2017
Enrollment StartNov 1, 2016
Primary CompletionMay 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 9.1 years ago

Interventions

mucosal impedance (MI) testingother

During routine colonoscopy, consented study participants will have a MI catheter sensor positioned along the mucosal wall to measure resistance across the mucosa. The physician will take measurements in each segment of the colon, including segments that appear inflamed and normal adjacent areas (up to 10 locations). To obtain a stable reading, the sensor must remain in contact with the mucosa for five seconds. The study procedure will add approximately 1-2 minutes of anesthesia time for each participant. Basic demographic information, prior IBD treatments, and prior colonoscopic data will be collected from the medical record following the procedure for those patients who consent to research.