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Follow-up study on the application of condylar constrained prosthesis TC3 in total knee arthroplasty

Follow-up study on the application of condylar constrained prosthesis TC3 in total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034640
Enrollment
Unknown
Registered
2020-07-12
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

knee joint disease

Interventions

A:primary TKA (with PFC Sigma TC3)
B:revision TKA (with PFC Sigma TC3)
C:TKA (primary or revision
with with PFC Sigma TC3 and mental pad)

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The patients used PFC Sigma TC3 in our department for complex primary or revision knee arthroplasty.

Exclusion criteria

Exclusion criteria: Patients lost to follow-up; Patients who refused to participate in the study

Design outcomes

Primary

MeasureTime frame
knee function;pain VAS score;Knee score;Patient satisfaction score;Quality of Life score;Imaging examination;—

Countries

China

Contacts

Public ContactZongke Zhou

West China Hospital, Sichuan University

zongke@126.com+86 13208193509

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026