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NCT02404545 · ClinicalTrials.gov registry record · NA
Prevention of Parastomal Hernia by Mesh Placement
A NA study, sponsored by University of Miami.
- Terminated
- Registry status
- NA
- Development phase
- 12
- Enrollment target
NCT02404545: Clinical Trial NA study, sponsored by University of Miami.
NCT02404545 is a NA study that was terminated before completion, run by University of Miami. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02404545, a NA study, was terminated before completion, sponsored by University of Miami.
- TERMINATED
- Registry status
- NA
- Development phase
- 12 participants
- Enrollment target
Study Summary
Concurrent placement of a mesh during formation of ileal conduit will decrease the incidence of parastomal hernia and associated complications.
Primary Outcome
Rate of reduction of the incidence of parastomal hernia in study participants, as assessed by physical examination
Interventions
- DEVICE Ethicon Physiomesh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2015-08-14 |
| Est. Completion | 2017-03 |
| Phase | NA |
Why NCT02404545 stopped before completion
NCT02404545 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 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Ethicon Physiomesh is the first listed.
NCT02404545 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02404545 about?
NCT02404545 is a clinical study titled "Prevention of Parastomal Hernia by Mesh Placement". Concurrent placement of a mesh during formation of ileal conduit will decrease the incidence of parastomal hernia and associated complications.
What is the current status of trial NCT02404545?
This trial is currently terminated. It is a NA study. The enrollment target is 12 participants. The study started on 2015-08-14. Estimated completion is 2017-03.
What interventions are being tested in trial NCT02404545?
The interventions under investigation include: Ethicon Physiomesh (DEVICE).
Who is sponsoring clinical trial NCT02404545?
This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02404545's enrollment target sits among peer trials
12 1913th of 2000 higher than 74 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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