Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh

NCT04779918 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 160 participants
Start Date 2021-04-29
Est. Completion 2027-12-30
Phase NA

Sponsor

Tela Bio

34 total trials

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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. 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 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tela Bio, which has 34 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. 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: NCT04779918 reports 10 study locations spanning 8 distinct geographic areas — top geographies include Florida, New York, Alabama. 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 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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04779918?

The interventions under investigation include: OviTex Reinforced Tissue Matrix (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04779918?

This trial is sponsored by Tela Bio, which has 34 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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