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Clinical Trials in China / NCT06617819
Starting soon Not applicable

Influence of Different Prostheses on Postoperative Clinical Function in Total Knee Arthroplasty

NCT06617819 · tracked via the Priya Life Science China tracker
Sponsor
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Phase
Not applicable
Started
2024-09-30
Last updated
2024-10-01

Condition(s) studied

Knee Arthropathy

Investigational drug(s) / intervention(s)

CR prosthesisPS prosthesis

CR prosthesis: For patients undergoing simultaneous bilateral knee arthroplasty, different prostheses (CR vs. PS) were randomized to the left or right knee.

PS prosthesis: For patients undergoing simultaneous bilateral knee arthroplasty, different prostheses (CR vs. PS) were randomized to the left or right knee.

Study summary

Exploring differences in knee function after surgery with different types of prostheses(Cruciate ligament retaining(CR) VS. posterior stabilizing(PS))

Eligibility

Sex
ALL
Min age
45 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age 45-80 years, any gender, BMI \< 35 kg/m2 2. Initial diagnosis of bilateral knee OA (Kellgren-Lawrence classification grades 3 or 4). Patients who are to undergo simultaneous primary bilateral knee arthroplasty 3. Inversion deformity ≤ 15° 4. Posterior cruciate ligament integrity Exclusion Criteria: 1. History of knee surgery (ligament, osteotomy, etc.) 2. knee flexion\<90°. 3. flexion contracture of one knee \> 10° 4. Comorbidity with other diseases, such as peripheral neuropathy, malignant tumors, rheumatism, etc. 5. Posterior cruciate ligament injury 6. Those assessed to be intolerant of surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University Nanjing Jiangsu

More The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06617819 on ClinicalTrials.gov ↗ ← All trials in China