Knee Injuries Clinical Trial
— CASHOfficial title:
Changes in the Immunomodulatory Properties of Adipose Stromal Cells Due to Hemarthrosis After Knee Injury
NCT number | NCT05687331 |
Other study ID # | NL77974.091.21 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | April 5, 2022 |
Est. completion date | April 1, 2024 |
The goal of this observational study is to gain insight in the natural course of pro-inflammatory factors and hemarthrosis in patients older than 18 with a recent knee trauma. The main question[s] it aims to answer are: - What is the natural course of pro-inflammatory factors and hemarthrosis in knee trauma? - What are the effects of inflammation and hemarthrosis on the anti-inflammatory potential of ASC's in order to better determine eligible patients and circumstances for ASC's therapy? Participants will: - undergo blood withdrawal - undergo knee arthrocentesis for synovial fluid sample collection - physical examination - fill out a questionnaire on knee complaints
Status | Recruiting |
Enrollment | 20 |
Est. completion date | April 1, 2024 |
Est. primary completion date | April 1, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Recently suffered an injury of the index knee (rotational or hyperextension) - A swollen joint - Inability to mobilise Exclusion Criteria: - Patients with an active inflammatory or infectious comorbid disease (including rheumatic diseases) - Patients using systemic immunosuppressant medication - Patients with a contra-indication for undergoing a MRI-scan (non-compatible implants or claustrophobia for example) - Patients with knee prosthesis - Patients with coagulation disorders - Patients with a history of a cruciate ligament or meniscal injury of the index knee - Patients with a tibiofemoral fracture of the index knee due to current distortion - In case the inclusion of the required amount of patient is reached in one the patient groups, additional patients belonging in the same patient group will not be included in the study |
Country | Name | City | State |
---|---|---|---|
Netherlands | Radboud umc | Nijmegen | Gelderland |
Lead Sponsor | Collaborator |
---|---|
Radboud University Medical Center |
Netherlands,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Synovial fluid analysis | Analysis of changes in pro-inflammatory factors, erythrocytes (as measurement for hemarthrosis) | Samples are taken at week 1, week 2, week 4, week 6 and week 8 after trauma | |
Secondary | co-culture of synovial fluid with adipose stromal cells | Assessment of changes in cytotoxity of hemarthrosis in synovial fluid on adipose stromal cells | samples are taken at week 1, week 2, week 4, week 6 and week 8 after trauma | |
Secondary | MRI-imaging | MRI-images to determine post-traumatic changes in the articulate cartilage | At inclusion and 1 year after trauma | |
Secondary | Physical examination | Assessment of changes in swelling, warmth and appearance of the skin | Physical examination at week 1, week 2, week 4, week 6 and week 8 after trauma | |
Secondary | Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire | Assessment changes of knee complaints by using the Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire, with minimum score of 0 and a maximum score of 100 and a higher score meaning a better outcome. | Questionnaires are taken at week 1, week 2, week 4, week 6 and week 8 after trauma |
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