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Clinical application effect of tension feedback system in robot assisted total knee arthroplasty

Clinical application effect of tension feedback system in robot assisted total knee arthroplasty

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096344
Enrollment
Unknown
Registered
2025-01-22
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Knee osteoarthritis

Interventions

Test group:Tension feedback system assisted robot total knee arthroplasty
control group:Robot-assisted total knee arthroplasty

Sponsors

Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age 50~80 years old, gender not limited; (2) Patients diagnosed with end-stage knee joint disease who have failed conservative treatment; (3) Patients assessed by researchers to require unilateral first knee replacement surgery; (4) The subjects/guardians are able to understand the purpose of the trial, demonstrate sufficient compliance with the trial protocol, and are willing to participate in this study and sign an informed consent form (ICF).

Exclusion criteria

Exclusion criteria: (1) Patients with neuromuscular dysfunction (such as paralysis, muscle dissolution) can experience postoperative functional impairment that affects lower limb function; (2) Patients with severe internal or surgical diseases or weak constitution who cannot tolerate surgery; (3) Tabetic arthropathy; (4) There are active infection foci in the body (systemic or local infection lesions); (5) Inflammatory joint disease leads to instability of the knee joint; (6) Previous trauma diagnosis of traumatic arthritis; (7) Postoperative patients undergoing knee joint ligament surgery; (8) Severe osteoporosis, metabolic bone disease, radiation bone disease, and tumors around the knee joint; (9) Patients with expected poor compliance; (10) Pregnant or lactating women, or patients with fertility plans during clinical studies; (11) Other situations that researchers consider unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
Medial and lateral space of knee joint;

Secondary

MeasureTime frame
Native tension of knee joint;Soft tissue tension inside and outside the knee joint;Knee Society Score;Western Ontario and McMaster Universities Osteoarthritis Index;Short Form 12 Health Survey;Forgotten Joint Score;Segmented surgical time;Surgical trauma indicators;Gait analysis examination;

Countries

China

Contacts

Public ContactZhang Yuan

The Second Affiliated Hospital of the Chinese People's Liberation Army Army Medical University

joint_chueng@hotmail.com+86 135 9401 0680

Outcome results

None listed

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