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JuggerStitch Post Market Clinical Follow-up Study

NCT04228367 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 104

Last updated 2025-11-12

No results posted yet for this study

Summary

This study is a post-market follow-up study. The data collected from this study will serve the purpose of confirming the safety and performance of the JuggerStitch Device used for meniscal repair according to the product labelling (Instruction For Use).

Conditions

  • Meniscus Tear, Tibial
  • Meniscus Lesion

Interventions

DEVICE

JuggerStitch Meniscal Repair Device

Treatment of torn meniscus with JuggerStitch.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Nesma Bayrich, DDS · Zimmer Biomet

  • Kim Blick · Zimmer Biomet

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-25
Primary Completion
2026-03-31
Completion
2026-04-30
FDA Device
Yes

Countries

  • United States
  • France
  • Germany
  • Japan

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 NCT04228367 on ClinicalTrials.gov