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NCT04779918 · ClinicalTrials.gov registry record · NA
Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh
A NA study of Hernia, Ventral and Hernia, Inguinal, sponsored by Tela Bio.
- Recruiting
- Registry status
- NA
- Development phase
- 160
- Enrollment target
- 10
- Study locations
NCT04779918 is a NA study of Hernia, Ventral and Hernia, Inguinal that is actively recruiting participants, run by Tela Bio. The registered enrollment target is 160 participants, roughly in line with the 161-participant average among 7 other Hernia, Ventral trials with a reported enrollment target. The trial reports 10 study locations across 8 states.
The verdict
NCT04779918, a NA study of Hernia, Ventral and Hernia, Inguinal, is actively recruiting participants, sponsored by Tela Bio.
- RECRUITING
- Registry status
- NA
- Development phase
- 160 participants
- Enrollment target
- 10
- Study locations
Study Summary
This study is designed to evaluate the post-operative complications and hernia recurrence following the use of OviTex in subjects with ventral or inguinal hernias. Up to 160 subjects will participate in the study from up to 20 investigator sites.
Conditions Studied
Interventions
- DEVICE OviTex Reinforced Tissue Matrix
Study Locations (10)
Florida
- GenesisCare - Destin
- Surgical Healing Arts Center - Fort Myers
New York
- St. Francis Hospital - Roslyn
- Mohawk Valley Health System - Utica
Alabama
- University of South Alabama - Mobile
Colorado
- SurgOne - Denver
Kansas
- St. Luke's Hospital - Overland Park
Kentucky
- University of Louisville - Louisville
Michigan
- Munson Healthcare - Traverse City
Texas
- Houston Methodist - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2021-04-29 |
| Est. Completion | 2027-12-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04779918
The ClinicalTrials.gov registry entry for NCT04779918 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 161-participant average among 7 other Hernia, Ventral trials with a reported enrollment target. The listed sponsor is Tela Bio, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Hernia, Ventral appearing as the primary indexed condition, and to 1 intervention - of which OviTex Reinforced Tissue Matrix is the first listed.
NCT04779918 reports 10 study locations spanning 8 distinct geographic areas - top geographies include Florida, New York, Alabama.
Frequently Asked Questions
What is clinical trial NCT04779918 about?
NCT04779918 is a clinical study titled "Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh". This study is designed to evaluate the post-operative complications and hernia recurrence following the use of OviTex in subjects with ventral or inguinal hernias. Up to 160 subjects will participate in the study from up to 20 investigator sites.
What is the current status of trial NCT04779918?
This trial is currently recruiting. It is a NA study. The enrollment target is 160 participants. The study started on 2021-04-29. Estimated completion is 2027-12-30.
What conditions does trial NCT04779918 study?
This clinical trial studies the following conditions: Hernia, Ventral, Hernia, Inguinal.
What interventions are being tested in trial NCT04779918?
The interventions under investigation include: OviTex Reinforced Tissue Matrix (DEVICE).
Who is sponsoring clinical trial NCT04779918?
This trial is sponsored by Tela Bio, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04779918 being conducted?
This trial has 10 study locations across Alabama, Colorado, Florida, Kansas, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.