Actively Recruiting
Evaluation of a New Bi-Condylar Total Knee Prosthesis (TKP) With All-Ceramic Friction (The Forgotten Knee)
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-01-15
5
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The results of TKP (Total Knee Prosthesis) are satisfactory but do not reach those of THP (Total Hip Prosthesis) in terms of indolence and function. By using an all-ceramic friction torque, identical to that of the hip, the promotor of this Clinical Investigation expects to obtain an improvement in term of indolence, ability to perform heavy activities, knee stability and an improvement in the long-term survival of TKP, while at the same time, a decrease in the rate of re-intervention in young patients.
CONDITIONS
Official Title
Evaluation of a New Bi-Condylar Total Knee Prosthesis (TKP) With All-Ceramic Friction (The Forgotten Knee)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Previously active adult under 70 years of age with disabling knee osteoarthritis resistant to medical treatments (anti-inflammatories, infiltrations, analgesics), with a frontal deformity < 10° for a primary implantation
- Written informed consent by the patient
- Patients affiliated to the French social security system
You will not qualify if you...
- Knee deformity > 10°
- Obesity (BMI > 30)
- Inflammatory rheumatism
- History of infection
- Poor skin coverage at the knee joint
- Known allergy to the materials used and/or anesthetic used in the surgery
- Repeated falls, major neurological disorders, mental or neuromuscular disorders which can be a source of post-operative complications
- Significant functional deficit of the collateral ligaments
- Positive serum or urine pregnancy test for woman with child bearing potential
- Pregnancy or within 48 hours post-partum or breast feeding women
- Phobic patient refusing to have an MRI
- Patient with a contraindication to have an MRI (active medical devices, metal implants, etc.)
- Patient under legal protection
- Patient participating in another Clinical Investigation
- Post fracture osteoarthritis
- Osteoporosis
- Anatomical configuration not allowing the implant to be fixed (depending on size constraints)
- Disabling comorbidity upon any resumption of physical activity
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hôpital Lariboisière
Paris, France, 75010
Actively Recruiting
Research Team
P
Pascal BIZOT, MD, Pr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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