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Patient-Specific Versus Conventional Instrumentation in TKA

NCT02002624 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 140

Last updated 2013-12-06

No results posted yet for this study

Summary

The aim of this prospective multicenter randomized clinical trial (RCT) is to compare the clinical and radiologic results of primary total knee arthroplasty (TKA) using patient-specific versus conventional instrumentation.

Conditions

  • Osteoarthritis, Knee

Interventions

DEVICE

PSI

DEVICE

Conventional instrumentation

Sponsors & Collaborators

  • Cochin Hospital

    lead AMBIG

Principal Investigators

  • Stephane Boisgard, MD, PhD · University Hospital, Clermont-Ferrand

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
2011-09-30
Primary Completion
2013-07-31
Completion
2013-07-31

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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 NCT02002624 on ClinicalTrials.gov