Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty

Status unconfirmed

Conditions studied: Osteoarthritis

In brief

The purpose of the study is to determine the clinical outcomes and survivorship of robotic-arm assisted medial bicompartmental knee arthroplasty at two, five, seven and ten years postoperative.

Key facts

Study ID

NCT03668704

Run by

St. Helena Hospital Coon Joint Replacement Institute

People needed

50

Starts

2013-04-01

Expected to finish

2026-04-01

Last updated by the study team

2018-09-13

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All patients over 21 years of age who underwent robotic-arm assisted medial bicompartmental arthroplasty by the investigating surgeon and received MCK implants and are at least 24 months post-operative.
• Patient has signed an IRB approved Informed Consent Form or with IRB approved waiver of written signed consent, patient has verbally consented to study participation.
• Patient is willing to comply with follow up

You may not qualify if…

• Patients will be excluded from participation in the study if they are cognitively unable to answer questions related to their index procedure and health quality of life forms.
• Patient had active infection
• Implants were implanted without bone cement
• Patients did not have sufficient bone stock to allow for insertion and fixation of components
• Patient did not have sufficient soft tissue integrity to allow for stability
• Patient had a neurological or muscular deformity that did not allow for control of the knee.

Where it is running

• St. Helena Hospital Coon Joint Replacement Institute — St. Helena, California, United States

Full record on ClinicalTrials.gov

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