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Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair
NCT05610267 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to collect additional safety data and demonstrate the performance of Integra Gentrix® Surgical Matrix for reinforcement of ventral hernia repairs.
Conditions Studied
Interventions
- DEVICE Retrospective chart review
Study Locations (1)
Florida
- Surgical Healing Arts Center — Fort Myers
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2022-11-22 |
| Est. Completion | 2022-12-28 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05610267
The ClinicalTrials.gov registry entry for NCT05610267 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Integra LifeSciences Corporation, which has 14 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Ventral Hernia appearing as the primary indexed condition, and to 1 intervention — of which Retrospective chart review is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05610267 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05610267 about?
NCT05610267 is a clinical study titled "Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair". The purpose of this study is to collect additional safety data and demonstrate the performance of Integra Gentrix® Surgical Matrix for reinforcement of ventral hernia repairs.
What is the current status of trial NCT05610267?
This trial is currently completed. The enrollment target is 28 participants. The study started on 2022-11-22. Estimated completion is 2022-12-28.
What conditions does trial NCT05610267 study?
This clinical trial studies the following conditions: Ventral Hernia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05610267?
The interventions under investigation include: Retrospective chart review (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05610267?
This trial is sponsored by Integra LifeSciences Corporation, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05610267 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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