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Predictors of Early Success From Circumferential Compression STITCH Meniscal Repairs

NCT03097744 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 23

Last updated 2020-09-07

No results posted yet for this study

Summary

This is a retrospective study of meniscal tear repairs at least one-year post repair status. All patients were treated with Ceterix NovoStitch devices. The primary objectives of this study are to assess the clinical repair success rate via reoperation and PROs at greater than 12 months.

Conditions

  • Knee Medial Meniscus Tears
  • Meniscus Lesion
  • Meniscus; Rupture, Bucket Handle
  • Meniscus Disorder

Interventions

DEVICE

Ceterix NovoStitch

The device allows the physician to place a circumferential compression stitch around meniscal tears. This stitch is placed by passing suture from the tibial side to the femoral side of the meniscus and across the tear. This allows compression across the entire tear surface.

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Principal Investigators

  • Kathryn Olson · Ceterix Orthopaedics

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2018-04-20
Completion
2018-04-20
FDA Device
Yes

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 NCT03097744 on ClinicalTrials.gov