Skip to content

Establishment and application of decision-making system based on AI+robot-assisted total knee arthroplasty

Establishment and application of decision-making system based on AI+robot-assisted total knee arthroplasty

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101314
Enrollment
Unknown
Registered
2025-04-23
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Osteoarthritis of the knee

Interventions

MA-TKA:Manual Total Knee Arthroplasty
FA-rTKA:AI-assisted robotic alignment for total knee arthroplasty

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Over 18 years old, no gender restriction; 2.Including patients who have undergone hip or knee arthroplasty and those scheduled to undergo robot-assisted knee arthroplasty. 3.Severe knee pain or other clinical symptoms, with a clear diagnosis of knee osteoarthritis, KL grade (Kellgren-Lawrence grading scale) III or IV, and ineffective conservative treatment. 4.RFA-TKA or MA-TKA. 5.Complete preoperative and postoperative general data, imaging data, and follow-up data, with a follow-up period of over 3 months. 6.Complete medical records, including surgical records, postoperative follow-up records, blood tests, nutritional status, and psychological health assessments. 7.Consent to provide personal medical information and comply with the research process.

Exclusion criteria

Exclusion criteria: 1.Patients lacking key clinical data or surgical information, or whose data quality does not meet the research requirements. 2.Diseases such as hemophilic arthritis or other conditions that severely affect postoperative rehabilitation. 3.History of fractures of the femur, tibia, fibula, or surrounding knee joint bones. 4.Preoperative anemia, coagulation dysfunction, or other primary or secondary hematologic disorders. 5.Current or past injuries to the knee's medial and lateral collateral ligaments or cruciate ligaments. 6.Poor compliance.

Design outcomes

Primary

MeasureTime frame
Postoperative pain;Postoperative function;Infection rate;Imaging results;Improvement in quality of life;

Secondary

MeasureTime frame
Blood indicators;

Countries

China

Contacts

Public ContactK LI

The First Affiliated Hospital of Chongqing Medical University

chrisli8929@live.cn+86 23 89011019

Outcome results

None listed

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