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RecruitingNeurogenic Bowel DysfunctionSpinal Cord Injury

Vibrant Capsule for Spinal Cord Injury Neurogenic Bowel Dysfunction

Eligible age

21+ yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

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

Sponsor: The University of Texas Health Science Center, Houston

You may qualify if…

  • 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.
  • Use of digital stimulation, suppositories, enemas, or mini enemas, as part of the scheduled bowel program.
  • Use of oral medications as part of the bowel program.

You may not qualify if…

  • Bowel incontinence occurring more than once per week.
  • Non-English-speaking individuals.
  • History of bowel obstruction, ileus, diverticulitis, or bowel surgery for a disease (appendix removal is ok).
  • Persistent autonomic dysreflexia (AD) triggered by bowel movements.
  • Recent changes to spasticity medications within the past month.
  • History of significant gastrointestinal disorders
  • History of Zenker's diverticulum
  • Dysphagia

Where it's recruiting

Texas

Houston

Source: ClinicalTrials.gov · NCT07213986 · last updated 2026-05-01