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Initial Safety Evaluation of FibroFix™ Meniscus

NCT02205645 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2019-03-13

No results posted yet for this study

Summary

Initial evaluation of safety and performance of FibroFix™ Meniscus scaffold

Conditions

  • Other Tear of Medial Meniscus, Current Injury

Interventions

DEVICE

FibroFix™ Meniscus scaffold

The test article for this study is the FibroFix™ Meniscus scaffold supplied by Orthox Ltd. The FibroFix™ Meniscus scaffold has been developed for repair of defects of the meniscus. The FibroFix™ Meniscus scaffold used in this study is a silk derived product developed to functionally replace the excised unstable meniscus following a meniscal tear.

Sponsors & Collaborators

  • Avon Orthopaedic Centre, North Bristol NHS Trust, Bristol UK

    collaborator UNKNOWN

  • University of Bristol

    collaborator OTHER

  • Orthox Limited

    lead INDUSTRY

Principal Investigators

  • Ashley Blom, Professor · University of Bristol

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2017-10-17
Completion
2017-10-17

Countries

  • United Kingdom

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 NCT02205645 on ClinicalTrials.gov