Inclusion criteria | |
 1. Grade II–III osteoarthritis, identified by two different observers, according to the Kellgren-Lawrence grading scale | |
 2. Hematological and biochemical analyses with no significant alterations that contraindicate intervention | |
 3. Aged 18 to 70 years old, males or females | |
 4. Diagnostic course of knee osteoarthritis for more than 6 months and less than 10 years | |
 5. An average pain intensity of grade 3 or more (less than 8) on a 10-point visual analog scale (VAS) | |
 6. Informed written consent provided by the patient | |
Exclusion criteria | |
 1. History of one or more drug allergies and two or more food allergies | |
 2. Obesity with a body mass index > 30 (calculated as mass in kg/height in m2) | |
 3. Neoplasia | |
 4. Signs of infection or positive serology for HIV, hepatitis, or syphilis | |
 5. Congenital or acquired diseases leading to significant knee deformities that may interfere with cell application or the interpretation of results | |
 6. Pregnancy or breastfeeding | |
 7. Immunosuppression | |
 8. Intra-articular injection of any drug during the previous 3 months | |
 9. Participation in another clinical trial or treatment with another investigational product within 30 days prior to inclusion in the study | |
 10. Other conditions that may, according to medical criteria, discourage participation in the study |