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A Single-center Randomized Controlled Trial to Evaluate the Effect on Postoperative Function of Patellar Resurfacing in Total Knee Arthroplasty

A Single-center Randomized Controlled Trial to Evaluate the Effect on Postoperative Function of Patellar Resurfacing in Total Knee Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011270
Enrollment
Unknown
Registered
2017-05-01
Start date
2017-06-01
Completion date
Unknown
Last updated
2017-05-09

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

Conditions

knee Osteoarthritis

Interventions

Intervention group:Patellar Resurfacing
Controlled group:No Patellar Resurfacing

Sponsors

Chinese People's Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 65 years old; 2. One-stage bilateral TKA with similar severity of both sides; 3. Informed consent was signed.

Exclusion criteria

Exclusion criteria: 1. Revised TKA; 2. Patients with severe heart, brain, liver, kidney dysfunction; 3. Severe deformity (varus angulation, valgus angulation, or flexion contracture of more than 15 degree); 4. Intra-operative complications affect postoperative recovery; 5. Patients with mental illness or acataphasia; 7. To participate in other clinic trials in two months; 8. Patients were unwilling to sign informed consent or to compliance trial program.

Design outcomes

Primary

MeasureTime frame
Knee Society Score;6 minutes walking test;

Secondary

MeasureTime frame
The location and degree of pain;

Countries

China

Contacts

Public ContactJiying Chen

Chinese People's Liberation Army General Hospital

jiyingchen_301@163.com+86 010-66875504

Outcome results

None listed

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