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A Longitudinal Prospective Outcomes Study of Laparoscopic Abdominal Wall Hernia Repair Using Symbotex™ Composite Mesh

NCT02341430 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2019-02-07

No results posted yet for this study

Summary

This study is being done to test the efficacy of Symbotex™ as an effective synthetic mesh option in the repair of grade I and II ventral hernias.

Conditions

  • Grade I Ventral Hernia
  • Grade II Ventral Hernia

Interventions

DEVICE

Symbotex™ Composite Mesh

Repair of a Grade I or II ventral hernia according to VHWG classification system with Symbotex™ Composite Mesh

Sponsors & Collaborators

  • Medtronic - MITG

    collaborator INDUSTRY

  • Anne Arundel Health System Research Institute

    lead OTHER

Principal Investigators

  • Adrian Park, M.D. · Anne Arundel Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
TRIPLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-09-11
Completion
2018-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02341430 on ClinicalTrials.gov