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Middle - and long-term follow-up cohort study for the clinical efficacy of restricted total knee prosthesis in the treatment of genu valgus deformity

Middle - and long-term follow-up cohort study for the clinical efficacy of restricted total knee prosthesis in the treatment of genu valgus deformity

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025661
Enrollment
Unknown
Registered
2019-09-04
Start date
2019-09-04
Completion date
Unknown
Last updated
2019-09-09

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

Conditions

Restricted total knee prosthesis

Interventions

Case series:Total knee-joint prostheses

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Valgus Angle >15 degree; 2. Initial total knee replacement; 3. The follow-up time was more than 1 year.

Exclusion criteria

Exclusion criteria: 1. The evaluation of knee joint affected by other diseases (such as spinal and hip diseases, etc.); 2. Cases lost to follow-up.

Design outcomes

Primary

MeasureTime frame
Prosthesis position;line of force;KSS score;WOMAC score;EQ-5D;Gait analysis;—

Countries

China

Contacts

Public ContactFeng Shuo

Affiliated Hospital of Xuzhou Medical University

781733181@qq.com+86 18552880088

Outcome results

None listed

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