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A single-blind randomized controlled study on the clinical efficacy of the "H" shaped position and conventional position for left total knee replacement surgery.

A single-blind randomized controlled study on the clinical efficacy of the "H" shaped position and conventional position for left total knee replacement surgery.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072953
Enrollment
Unknown
Registered
2023-06-28
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Total knee Arthroplasty

Interventions

The "H" shaped position group.:H-shaped position group (Group A), in which patients use the H-shaped position before surgery, and the same right-handed surgeon performs the entire surgery
Control group:Left total knee Joint replacement in normal position

Sponsors

The Second People's Hospital of Shenzhen.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with left knee osteoarthritis (KOA). 2. Aged between 60 and 80 years. 3. The patient's knee joint is classified as Grade III or IV according to the K-L grading system on imaging. 4. The patient's knee joint functional score is HSS=40, quality of life score is SF-36=20, pain score is VAS=6, and the patient expresses a clear surgical intention. 5. The patient agrees to participate in the study and signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with rheumatoid knee arthritis, traumatic knee arthritis, and other non-degenerative joint diseases. 2. Patients requiring revision surgery after total knee replacement due to factors such as infection, prosthesis loosening, and periprosthetic fracture. 3. Patients with coagulation function disorders and high-risk bleeding during perioperative period. 4. Patients requiring complex prosthesis replacement due to various reasons. 5. Patients who did not successfully complete the surgery. 6. Patients who are unable to comply with postoperative follow-up and rehabilitation training.

Design outcomes

Primary

MeasureTime frame
KSS score at 12 weeks after surgery.;

Secondary

MeasureTime frame
Postoperative alignment of the force line and the angle of knee joint varus or valgus.;Lower limb thrombosis.;Postoperative pain VAS score.;Postoperative complications.;

Countries

China

Contacts

Public ContactShang Hongxi

The Second People's Hospital of Shenzhen.

shanghongxi@sina.com+86 136 3166 2918

Outcome results

None listed

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