Compares treatment options for Total Knee Replacement
Official title Comparison of Pivotal Medial Polyethylene Versus Ultra-congruent in Total Knee Arthroplasty
ClinicalTrials.gov ID: NCT06676189
What this study is testing
- What it's testing
- The aim of this study is to compare the forgotten joint score for the medial pivot polyethylene and ultra-congruent polyethylene which are used in total prosthetic replacement of the knee
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 90
You may be able to join if
- people 18 to 90 years of age, eligible for a primary total knee replacement for gonarthrosis
- Competent people able to give informed consent to participate in the research
- Affiliation to the social security system
You likely can't join if
- Infection history of the knee to be replaced
- Deformity greater than 15 degrees
- Any surgical and/or anesthetic contraindication, or any condition deemed by the investigator to be incompatible with the research.
- Any contraindication mentioned in the instructions for use of the medical device
- Pregnant or breastfeeding women
- Recent infection history of the surgical site
See the full eligibility criteria
- people 18 to 90 years of age, eligible for a primary total knee replacement for gonarthrosis
- Competent people able to give informed consent to participate in the research
- Affiliation to the social security system
- Infection history of the knee to be replaced
- Deformity greater than 15 degrees
- Any surgical and/or anesthetic contraindication, or any condition deemed by the investigator to be incompatible with the research.
- Any contraindication mentioned in the instructions for use of the medical device
- Pregnant or breastfeeding women
- Recent infection history of the surgical site
- Adults who are subject to a legal protection measure or who are unable to express their constent (Article L1121-8 of the French Public Health Code) and people under judicial protection (article L. 1122-2 FPHC)
- people who refuse to participate
The study team makes the final eligibility decision.
Where it's taking place
- Clermont-Ferrand, France
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 90 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Clermont-Ferrand, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.