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Association between preoperative thigh muscle mass and outcomes after TKA in patients with hemophilic knee arthritis

Association between preoperative thigh muscle mass and outcomes after TKA in patients with hemophilic knee arthritis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120082
Enrollment
Unknown
Registered
2026-03-09
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Hemophilic arthritis

Interventions

Hemophilic Knee Osteoarthritis Group (KHA Group):None
Knee Osteoarthritis Group (KOA Group):None

Sponsors

The Third Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
22 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. KHA Group Inclusion Criteria (1) Age 18-65 years; meet "Chinese Expert Consensus on Diagnosis and Treatment of Hemophilia (2021 Edition)"; confirmed hemophilia A/B diagnosis; unilateral or bilateral knee involvement (confirmed by physical exam and knee X-ray showing arthritis features, Arnold-Hilgartner score grade IV or higher); (2) Knee disease duration >=1 year; (3) No acute knee hemorrhage in the past 2 weeks; (4) Undergoing unilateral total knee arthroplasty (TKA); (5) Capable of independently completing CT examination and lower limb functional assessment. 2. KOA Group Inclusion Criteria (1) 1:1 individual matching with KHA group (matching criteria: same gender, BMI +/-2.0 kg/m^2); (2) Meet American College of Rheumatology (ACR) osteoarthritis diagnostic criteria; knee X-ray Kellgren-Lawrence (K-L) grade 3-4; (3) Knee disease duration >=1 year; (4) No acute knee pain episode in the past 2 weeks (VAS pain score <=5); (5) Capable of independently completing imaging and functional assessment.

Exclusion criteria

Exclusion criteria: 1. History of previous surgery on the same-side knee; 2. Coexisting neuromuscular diseases, spinal cord injury, or cerebral infarction; 3. Coexisting severe liver or kidney dysfunction, malignant tumors, or heart failure; 4. Inability to complete follow-up assessments.

Design outcomes

Primary

MeasureTime frame
Skeletal muscle volume (MV);Skeletal muscle quality (SMF);Intermuscular adipose tissue volume (IMAT);Subcutaneous adipose tissue volume (SAT);Knee Society Score (KSS);Short Form-12 Health Survey (SF-12) score;Harris Hip Joint Score (HJHS);Active range of motion (ROM) of the knee joint;

Countries

China

Contacts

Public ContactFeng Rui

The Third Affiliated Hospital of Guangzhou University of Chinese Medicine

19313015947@163.com+86 755 28282222

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026