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Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty

NCT03106558 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2017-04-10

No results posted yet for this study

Summary

This is an early user evaluation of the robotic-assisted total knee arthroplasty platform. The objective of this surgeon group is to capture data on the defined objectives and provide Stryker with feedback.

Conditions

  • Osteoarthritis, Knee

Interventions

DEVICE

Total Knee Arthroplasty using Manual Instrumentation

DEVICE

Total Knee Arthroplasty using Robotic Arm

Sponsors & Collaborators

  • Stryker Orthopaedics

    collaborator INDUSTRY

  • Rothman Institute Orthopaedics

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2019-06-30
Completion
2019-06-30
FDA Device
Yes

Countries

  • United States

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 NCT03106558 on ClinicalTrials.gov