Vibrant Capsule for Spinal Cord Injury Neurogenic Bowel Dysfunction

Part of paid clinical trials in Houston, Texas.

Sponsor
The University of Texas Health Science Center, Houston
Study ID
NCT07213986
Status
Recruiting
Apply to this trial

Conditions

  • Neurogenic Bowel Dysfunction
  • Spinal Cord Injury

Eligibility Criteria

Sex
ALL
Age
21 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Vibrant Capsule — DEVICE
    The Vibrant capsule is designed to alleviate chronic constipation by stimulating the colon through gentle vibrations. The Vibrant capsule will be swallowed and tracked through the digestive system of spinal cord injury patients.

Study Details

The goal of this study is to test the safety and effectiveness of Vibrant capsules in spinal cord injury patients with neurogenic bowel.

Key Dates

Start date
Jan 6, 2026
Status verified
Apr 2026
Primary completion
Aug 19, 2026
Completion
Aug 19, 2026

Study Design

Enrollment
12 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Vibrant Capsule

Primary Outcome Measure

Safety of Vibrant capsule as indicated by number of participants who had an adverse event [ Time Frame: baseline week 1, baseline week 2, baseline week 3, baseline week 4 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
TIRR Memorial HermannHoustonTexas77030
Danira Garcia Gutierrez, BS
[email protected]
713-797-7133
Jacqueline B Martinez, BS
[email protected]
7137975765
Argyrios Stampas, MD (PRINCIPAL_INVESTIGATOR)

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By research site
TIRR Memorial Hermann· Houston, TX

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