Actively Recruiting
Clinical Cohort Study of Knee Arthroplasty Assisted by Digital Technology
Led by Tian Hua · Updated on 2023-08-25
12000
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Through this cohort study, previous clinical data can be systematically reviewed and supplemented through clinical follow-up. Prospective enrollment and follow-up observation of subsequent patients can also be carried out to build a retrospective-prospective two-way cohort study. The intraoperative, perioperative, clinical follow-up and health economics of surgical robot, computer navigation, personalized osteotomy guide and other digital technologies and traditional TKA were comprehensively and objectively compared, the results and conclusions of the center were summarized and reported, and the effectiveness and safety of digital assistive technology applied to TKA were explored, providing references for clinical diagnosis and follow-up research.
CONDITIONS
Official Title
Clinical Cohort Study of Knee Arthroplasty Assisted by Digital Technology
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary knee osteoarthritis
- Unilateral primary knee replacement
- Surgical methods include traditional surgery, surgical robot, computer navigation, or personalized osteotomy guide
You will not qualify if you...
- History of renal insufficiency (creatinine > 2.5), liver insufficiency, severe heart disease or coronary stenting within the last 12 months
- Severe respiratory disease
- History of venous thromboembolism or high risk of thrombosis (hereditary or acquired)
- Coagulation disorder
- Stroke
- Malignancy
- Refusal to participate or unwillingness to sign informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Peking University Third Hospital
Beijing, Beijing Municipality, China, 100181
Actively Recruiting
Research Team
T
Tian Hua, MD
CONTACT
Z
Zheng Yuhang, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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