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NCT03091790 · ClinicalTrials.gov registry record · NA
Mesh Type in Ventral Hernia Repair
A NA study of Ventral Hernia, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- NA
- Development phase
- 87
- Enrollment target
- 1
- Study location
NCT03091790 is a NA study of Ventral Hernia that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 87 participants, below the 138-participant average among 18 other Ventral Hernia trials with a reported enrollment target (37% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03091790, a NA study of Ventral Hernia, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- NA
- Development phase
- 87 participants
- Enrollment target
- 1
- Study location
Study Summary
Ventral hernias are common following abdominal surgery. Currently, there is no equipoise on when synthetic and biologic meshes should be used. Among open ventral hernia repairs, half are repaired using biologic mesh while half are repaired using synthetic mesh. The investigators hypothesize that biologic mesh as opposed to synthetic mesh repair of open ventral hernia repair is associated with decreased risk of major complications one year after surgery.
Conditions Studied
Interventions
- DEVICE Synthetic Mesh
- DEVICE Biologic Mesh
Study Locations (1)
Texas
- UT Health at Lyndon B. Johnson General Hospital - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 87 participants |
| Start Date | 2017-03-27 |
| Est. Completion | 2021-07-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03091790
The ClinicalTrials.gov registry entry for NCT03091790 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 87 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 138-participant average among 18 other Ventral Hernia trials with a reported enrollment target (37% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Ventral Hernia appearing as the primary indexed condition, and to 2 interventions - of which Synthetic Mesh is the first listed.
NCT03091790 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT03091790 about?
NCT03091790 is a clinical study titled "Mesh Type in Ventral Hernia Repair". Ventral hernias are common following abdominal surgery. Currently, there is no equipoise on when synthetic and biologic meshes should be used. Among open ventral hernia repairs, half are repaired using biologic mesh while half are repaired using synthetic mesh. The investigators hypothesize that bio...
What is the current status of trial NCT03091790?
This trial is currently completed. It is a NA study. The enrollment target is 87 participants. The study started on 2017-03-27. Estimated completion is 2021-07-31.
What conditions does trial NCT03091790 study?
This clinical trial studies the following conditions: Ventral Hernia.
What interventions are being tested in trial NCT03091790?
The interventions under investigation include: Synthetic Mesh (DEVICE), Biologic Mesh (DEVICE).
Who is sponsoring clinical trial NCT03091790?
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 NCT03091790 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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Read our methodology - how this data is sourced, computed, and verified.
Related
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