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NCT07213986 · ClinicalTrials.gov registry record · NA
Vibrant Capsule for Spinal Cord Injury Neurogenic Bowel Dysfunction
A NA study of Spinal Cord Injury and Neurogenic Bowel Dysfunction, sponsored by The University of Texas Health Science Center, Houston.
- Recruiting
- Registry status
- NA
- Development phase
- 12
- Enrollment target
- 1
- Study location
NCT07213986: Recruiting NA study of Spinal Cord Injury and Neurogenic Bowel Dysfunction, sponsored by The University of Texas Health Science Center, Houston.
NCT07213986 is a NA study of Spinal Cord Injury and Neurogenic Bowel Dysfunction that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 12 participants, below the 86-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07213986, a NA study of Spinal Cord Injury and Neurogenic Bowel Dysfunction, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.
- RECRUITING
- Registry status
- NA
- Development phase
- 12 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this study is to test the safety and effectiveness of Vibrant capsules in spinal cord injury patients with neurogenic bowel.
Conditions Studied
Interventions
- DEVICE Vibrant Capsule
Study Locations (1)
Texas
- TIRR Memorial Hermann - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2026-01-06 |
| Est. Completion | 2026-03-01 |
| Phase | NA |
What NCT07213986 shows while recruiting
NCT07213986 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 86-participant average among 99 other Spinal Cord Injury trials with a reported enrollment target (86% lower).
The record links to 2 conditions, with Spinal Cord Injury appearing as the primary indexed condition, and to 1 intervention - of which Vibrant Capsule is the first listed.
NCT07213986 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT07213986 about?
NCT07213986 is a clinical study titled "Vibrant Capsule for Spinal Cord Injury Neurogenic Bowel Dysfunction". The goal of this study is to test the safety and effectiveness of Vibrant capsules in spinal cord injury patients with neurogenic bowel.
What is the current status of trial NCT07213986?
This trial is currently recruiting. It is a NA study. The enrollment target is 12 participants. The study started on 2026-01-06. Estimated completion is 2026-03-01.
What conditions does trial NCT07213986 study?
This clinical trial studies the following conditions: Spinal Cord Injury, Neurogenic Bowel Dysfunction.
What interventions are being tested in trial NCT07213986?
The interventions under investigation include: Vibrant Capsule (DEVICE).
Who is sponsoring clinical trial NCT07213986?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07213986 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT07213986's enrollment target sits among peer trials
12 73rd of 99 higher than 21 of 99 other Spinal Cord Injury trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Spinal Cord Injury trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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