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Comparison Between Velys J&J Robotic-assisted and Cori S&N Robotic-assisted Total Knee Arthroplasty

Comparison Between Velys J&J Robotic-assisted and Cori S&N Robotic-assisted Total Knee Arthroplasty

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07555067
Acronym
TKA
Enrollment
200
Registered
2026-04-28
Start date
2026-01-01
Completion date
2027-03-01
Last updated
2026-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Arthritis Osteoarthritis

Brief summary

This randomised controlled trial will include patients with end-stage osteoarthritis of the knee undergoing primary TKR. Patients meeting the criteria that consent to be in the study will be randomised at a ratio of 1:1 to either Velys J&J robotic-assisted or Cori S&N robotic-assisted TKR. The primary objective will assess pre- and postoperative HKA angle, CPAK and range of motion using goniometer to compare two groups.The secondary objectives are to compare patient expectation, functional ability, quality of life using functional 48-point Oxford Knee Score and Forgotten joint score.

Detailed description

This randomised controlled trial will include patients with end-stage osteoarthritis of the knee undergoing primary TKR. Patients meeting the criteria that consent to be in the study will be randomised at a ratio of 1:1 to either Velys J&J robotic-assisted or Cori S&N robotic-assisted TKR. The primary objective will assess pre- and postoperative HKA angle, CPAK and range of motion using goniometer to compare two groups.The secondary objectives are to compare patient expectation, functional ability, quality of life using functional 48-point Oxford Knee Score and Forgotten joint score.

Interventions

assess preoperative HKA

asses preoperative CPAK

assess preoperative Oxford Knee Score

assess preoperative Forgotten Joint Score

assess preoperative range-of-motion

postoperative HKA

postoperative CPAK

postoperative range-of-motion

postoperative Oxford Knee Score

postoperative Forgotten Joint Score

Sponsors

Jan Biziel University Hospital No 2 in Bydgoszcz
Lead SponsorOTHER
Vascular surgery, University hospital Královské Vinohrady, Prague
CollaboratorOTHER
Charles University, Czech Republic
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

gonarthrosis

Exclusion criteria

heavy systemic diseases

Design outcomes

Primary

MeasureTime frame
1. HKA anglebefore and 3,6,12 after surgery
CPAKbefore and 3,6,12 months after surgery
range-of-motionbefore and 3,6,12 moths after surgery

Secondary

MeasureTime frame
Oxford Knee Scorebefore and 3,6,12 months after surgery
Forgotten Joint Scorebefore and 3,6,12 moths after surgery

Countries

Poland

Contacts

PRINCIPAL_INVESTIGATORMichał Kułakowski, PhD

Dr. Jan Biziel University Hospital No. 2 in Bydgoszcz

PRINCIPAL_INVESTIGATORJakub Błaszczyk

Dr. Jan Biziel University Hospital No. 2 in Bydgoszcz

PRINCIPAL_INVESTIGATORKarol Elster, PhD

Dr. Jan Biziel University Hospital No. 2 in Bydgoszcz

PRINCIPAL_INVESTIGATORJiří PhD Skála-Rosenbaum

Vascular surgery, University hospital Královské Vinohrady, Prague

PRINCIPAL_INVESTIGATORJakub Maléř

Vascular surgery, University hospital Královské Vinohrady, Prague

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026