Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
NA
80 participants
INTERVENTIONAL
2017-01-04
2028-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Substitution of the PCL in TKA With UC or PS Design
NCT04679857
Clinical Outcome After Total Knee Arthroplasty Using CR or PS Inlay
NCT03873363
Outcomes Following Total Knee Arthroplasty
NCT02364011
Metal Ion Concentration Between Coated and Uncoated TKA
NCT03047564
Rehabilitation After Fast-track Total Knee Arthroplasty
NCT01329081
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Coated Total Knee Arthroplasty
Implantation coated Total Knee Arthroplasty
Coated Total Knee Arthroplasty
Implantation coated Total Knee Arthroplasty
Standard Total Knee Arthroplasty
Implantation Standard Total Knee Arthroplasty
Standard Total Knee Arthroplasty
Implantation StandardTotal Knee Arthroplasty
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Coated Total Knee Arthroplasty
Implantation coated Total Knee Arthroplasty
Standard Total Knee Arthroplasty
Implantation StandardTotal Knee Arthroplasty
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* understanding of german language
Exclusion Criteria
* existence of other joint implants
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Technische Universität Dresden
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jörg Lützner, MD
Role: PRINCIPAL_INVESTIGATOR
University Center of Orthopaedics and Traumatology, University Medicine Carl Gustav Carus Dresden
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Center of Orthopaedics and Traumatology, University Medicine Carl Gustav Carus Dresden, TU Dresden
Dresden, Saxony, Germany
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Tille E, Beyer F, Lutzner C, Postler A, Thomas P, Summer B, Lutzner J. No difference in patient reported outcome and inflammatory response after coated and uncoated total knee arthroplasty - a randomized controlled study. BMC Musculoskelet Disord. 2023 Dec 14;24(1):968. doi: 10.1186/s12891-023-07061-x.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TKA cytokine
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.