Clinical and Radiological Results in Robotic Assisted Knee Prosthetic Surgery With ROSA® Knee System

Borja Alcobía-Díaz MD, PhD

Status: Unknown

Conditions: Robotic Assistance; Knee Prosthetic Surgery

Treatments: Device: ROSA® System Robotic Assisted Knee Prosthetic Surgery

Study type: Interventional

Funder types: Other

Identifiers

NCT05365022

22/081-EC_P

Details and patient eligibility

About

Comparing clinical and radiological results of patients after prosthetic surgery conventionally with no robotic assistance and ROSA® Knee prosthetic surgery robotic assistance.

Enrollment: 144 estimated patients

Sex: All

Ages: 40+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Knee osteoarthritis requiring PS Knee Prosthesis

Exclusion criteria

• Not meeting Inclusion Criteria
• Requiring Constrained Prosthesis
• Metal Allergy
• Neurological disorders.
• Cognitive impairment
• Not giving consent.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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144 participants in 2 patient groups

Conventional Non-Robotic Assisted Knee Prosthetic Surgery

No Intervention group

ROSA® System Robotic Assisted Knee Prosthetic Surgery

Active Comparator group

Treatment:

Device: ROSA® System Robotic Assisted Knee Prosthetic Surgery