Status:
ACTIVE_NOT_RECRUITING
Clinical Outcome After Total Knee Arthroplasty Using CR or PS Inlay
Lead Sponsor:
Technische Universität Dresden
Conditions:
Knee Osteoarthritis
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Compare knee flexion after cruciate-retaining and cruciate substituting Total Knee Arthroplasty.
Detailed Description
The aim of this study is to compare knee Flexion after cruciate-retaining (CR) and cruciate-substituting (posterior stabilized - PS) Total Knee Arthroplasty (TKA). For this purpose, flexion and exten...
Eligibility Criteria
Inclusion
- Indication for TKA with a non-linked, bicondylar total knee replacement
- written informed consent
Exclusion
- Chronic pain patients
- Neuromuscular Diseases
- general illnesses that make mobilisation more difficult and/or prevent follow-up
- Known posterior cruciate ligament insufficiency
- Need for a higher degree of linkage
- BMI over 40 kg/m²
- Study doctor, his family, employees or other dependent persons
Key Trial Info
Start Date :
April 1 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2030
Estimated Enrollment :
140 Patients enrolled
Trial Details
Trial ID
NCT03873363
Start Date
April 1 2018
End Date
September 1 2030
Last Update
February 20 2024
Active Locations (1)
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1
University Center of Orthopaedics and Traumatology, University Medicine Carl Gustav Carus Dresden, TU Dresden
Dresden, Saxony, Germany, 01307