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Mesh Suture for Internal Load Bearing Closures

NCT03940560 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2023-12-15

No results posted yet for this study

Summary

Determine whether Mesh Suture achieves an acceptable safety and efficacy profile in load bearing internal tissue approximations. Mesh Suture has a novel design that permits tissue ingrowth and limits suture pull-through--items important for internal high-tension repairs

Conditions

  • Suture; Complications, Mechanical
  • Suture; Complications, Infection or Inflammation
  • Suture, Complication

Interventions

DEVICE

Duramesh Suturable Mesh

Use of Duramesh Suturable Mesh for internal load bearing closures

Sponsors & Collaborators

  • Wigmore Clinic

    lead OTHER

Principal Investigators

  • Garen Koloyan, MD PhD · Wigmore Clinic

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-01
Primary Completion
2024-12-31
Completion
2025-12-31
FDA Device
Yes

Countries

  • Armenia

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 NCT03940560 on ClinicalTrials.gov