Fully Disposable Patient-Specific Instrumentation

NCT02966613 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 210

Last updated 2016-11-17

No results posted yet for this study

Summary

To evaluate the lower limb alignment following total knee arthroplasty (TKA) performed with fully disposable patient-specific instrumentation versus conventional, versus patient specific instrumentation.

Conditions

  • Osteoarthritis,Knee

Interventions

DEVICE

GMK Medacta Total Knee arthroplasty

Total Knee arthroplasty

Sponsors & Collaborators

  • Cochin Hospital

    lead AMBIG

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-12-31
Completion
2016-09-30

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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 NCT02966613 on ClinicalTrials.gov