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COMPLETED NA

A Comparison of Fortiva and Strattice Tissue Matrices in Complex, Ventral Hernia Repair

NCT02587403 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study is to compare the effectiveness of Fortiva Porcine Dermis versus Strattice Reconstructive Tissue Matrix for the underlay reinforcement of complex ventral hernia repair and assess post-operative complication rates, long term hernia recurrence rates.

Conditions Studied

Interventions

  • DEVICE Fortiva™ Porcine Dermis
  • DEVICE Strattice™ Reconstructive Tissue Matrix

Study Locations (1)

Missouri

  • Washington University — St Louis

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2015-12-02
Est. Completion 2023-09-19
Phase NA

Sponsor

RTI Surgical

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02587403

The ClinicalTrials.gov registry entry for NCT02587403 describes a study currently listed as completed. It is categorized as NA, 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 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is RTI Surgical, which has 4 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 2 interventions — of which Fortiva™ Porcine Dermis 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: NCT02587403 reports 1 study location spanning 1 distinct geographic area — top geographies include Missouri. 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 NCT02587403 about?

NCT02587403 is a clinical study titled "A Comparison of Fortiva and Strattice Tissue Matrices in Complex, Ventral Hernia Repair". The objective of this study is to compare the effectiveness of Fortiva Porcine Dermis versus Strattice Reconstructive Tissue Matrix for the underlay reinforcement of complex ventral hernia repair and assess post-operative complication rates, long term hernia recurrence rates.

What is the current status of trial NCT02587403?

This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2015-12-02. Estimated completion is 2023-09-19.

What conditions does trial NCT02587403 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 NCT02587403?

The interventions under investigation include: Fortiva™ Porcine Dermis (DEVICE), Strattice™ Reconstructive Tissue Matrix (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02587403?

This trial is sponsored by RTI Surgical, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02587403 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial