Active, not recruitingNo phase
Clinical Outcome After Total Knee Arthroplasty Using CR or PS Inlay
Key facts
- Who runs it
- Technische Universität Dresden
- Where
- Germany1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Active, not recruiting
- People taking part
- 140 people, planned
- Started
- 1 Apr 2018
- Expected to end
- 1 Sept 2030
- Type of study
- Interventional, 2 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- PS TKA
- CR TKA
- Record updated
- 20 February 2024
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 9 criteriaShow less
Who can take part
- Indication for TKA with a non-linked, bicondylar total knee replacement
- written informed consent
Who cannot take part
- Neuromuscular Diseases
- general illnesses that make mobilisation more difficult and/or prevent follow-up
- Known posterior cruciate ligament insufficiency
- Chronic pain patients
- Need for a higher degree of linkage
- BMI over 40 kg/m²
- Study doctor, his family, employees or other dependent persons
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
Compare knee flexion after cruciate-retaining and cruciate substituting Total Knee Arthroplasty.
The 2 groups in the trial
- PSTreatment being tested
Implantation of a posterior stabilized (cruciate substituting) Total Knee Arthroplasty.
Treatment: PS TKA
- CRExisting treatment, for comparison
Implantation of a cruciate retaining Total Knee Arthroplasty.
Treatment: CR TKA
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Prospective Randomized Comparison of Cruciate-retaining and Cruciate Substituting Surgical Technique for Total Knee Arthroplasty
- Record updated
- 20 February 2024