Status: Recruiting
A Prospective Trial of a Variable Compression System for Moderate to Severe Irritable Bowel Syndrome
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.
Participants needed: 20
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: PGP HealthUpdated: Apr 29, 2026Locations: 3
Eligibility criteria
Written informed consent to participate in the trial as prescribed. [+2]
Allergy to the investigational device or any components or clinically significan... [+7]