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Investigation of a Customized Femoral Resurfacing Implant

NCT01690689 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2020-12-17

No results posted yet for this study

Summary

The purpose is to assess the safety profile and performance of a femoral resurfacing implant for localized chondral lesions.

Conditions

  • Articular Cartilage Disorder

Interventions

DEVICE

Implant surgery

surgery

Sponsors & Collaborators

  • Episurf Medical Inc.

    lead INDUSTRY

Principal Investigators

  • Frederick Zetterberg · Episurf Medical

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2017-03-31
Completion
2017-03-31

Countries

  • Sweden

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 NCT01690689 on ClinicalTrials.gov