VCS Device Trial for Irritable Bowel Syndrome
Summary
NIH has registered a prospective interventional pilot trial (NCT07540312) to evaluate the safety and effectiveness of the Variable Compression System (VCS) device for treating moderate to severe Irritable Bowel Syndrome. The trial will enroll 20 subjects required to wear the device for a minimum of 6 hours daily, with follow-up assessments at 21 days, 8 weeks, and 6 months post-device administration.
What changed
NIH registered a new clinical trial on ClinicalTrials.gov for the Variable Compression System device in IBS patients. The trial is prospective and interventional, enrolling 20 subjects who must wear the device at least 6 hours daily, with follow-up visits at three intervals.
For medical device manufacturers and clinical investigators, this registration signals an active pathway to clinical evidence generation for non-pharmacological IBS treatments. Sponsors considering similar device-based IBS interventions should note the pilot study parameters as a benchmark for trial design and subject burden expectations.
Archived snapshot
Apr 21, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
A Prospective Trial of a Variable Compression System for Moderate to Severe Irritable Bowel Syndrome
N/A NCT07540312 Kind: NA Apr 20, 2026
Abstract
This prospective, interventional trial is intended to determine the safety and effectiveness of the Variable Compression System (VCS) device for Irritable Bowel Syndrome (IBS). This pilot study will enroll 20 subjects who will be required to wear the VCS device for a minimum of 6 hours a day and follow up at 21 days, 8 weeks, and 6 months post-device administration.
Conditions: IBS (Irritable Bowel Syndrome)
Interventions: Variable Compression System
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