Vibrant Capsule for Spinal Cord Injury Neurogenic Bowel Dysfunction

Recruiting N/A Interventional Study
Neurogenic Bowel Dysfunction Spinal Cord Injury
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
21 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
12 (estimated)
Sponsor
The University of Texas Health Science Center, Houston · Other
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About This Trial

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

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Individuals with chronic spinal cord injury (SCI) of more than one year. * Stable neurological level and function of SCI for at least six months. * Consistent bowel program without changes for at least 3 months. * At least one scheduled bowel movement (BM) every three days. * …
Contacts

Argyrios Stampas, MD

7127975938

argyrios.stampas@uth.tmc.edu

CONTACT

Danira Garcia Gutierrez, BS

7137977133

CONTACT