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Orthobiologic Treatment for Knee Osteoarthritis (Ortobiologisk Behandling av Kneleddsartrose)
The goal of this randomized clinical trial is to compare treatment for osteoarthritis in the knee using platelet rich plasma (PRP) or adipose stem cells (ADS). The main questions it aims to answer are: * Will the patients clinically benefit from the treatment, and if so, which treatment is better? * Will there be radiological findings to support this? Participants will be randomized into one of four groups: PRP, ADS, PRP + ADS or placebo treatment (saline) and will be examined and get an X-ray and MRI of the knee taken at inclusion and after 1 and 2 years.
Patients will be randomized into one of four treatment groups and then be followed up at 6 weeks, 12 weeks, 6 months, 1 year and 2 years after intervention. They will fill out scores and be clinically evaluated, as well as radiologically examined at inclusion and at the final check up (x-ray and MRI).
Age
40 - 70 years
Sex
ALL
Healthy Volunteers
No
University Hospital in Northern Norway
Tromsø, Tromsø, Norway
Start Date
September 23, 2024
Primary Completion Date
December 1, 2025
Completion Date
December 1, 2027
Last Updated
March 25, 2025
160
ESTIMATED participants
PRP injection
BIOLOGICAL
ADSTEM Inj. (Adult human mesenchymal stem cells)
BIOLOGICAL
Injection
BIOLOGICAL
Saline (NaCl 0,9 %) (placebo)
BIOLOGICAL
Lead Sponsor
University Hospital of North Norway
NCT06944808
NCT04782167
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT02285725