Saline Lavage X Saline Lavage and Osteonil® Mini in Rizarthritis
Rhizarthrosis, Metabolic Disease
About this trial
This is an interventional treatment trial for Rhizarthrosis focused on measuring carpometacarpal joint ostearthritis, hyaluronic acid, Rhizarthrosis
Eligibility Criteria
Inclusion Criteria:
- Men and women diagnosed with multiple arthritis (including CMC OA of the thumb) with comorbidities (metabolic syndrome, i.e., OA and overweight / obesity, and/or hyperglycemia, and/or dyslipidemia, and/or hyperuricemia, and/or hypertension).
- CMC OA joint of the thumb stages I to III as classified by Eaton et al. (4)
Exclusion Criteria:
- Missing classes or functional evaluations
- Not performing the exercises as instructed
Sites / Locations
- Instituto de Ortopedia e Traumatologia
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Lavage with Saline (LS)
Lavage with Osteonil® Mini (LO)
Under sterile conditions, the 1st carpometacarpal (CMC) will be locally anesthetized with ropivacaine and will be submitted to joint lavage with physiologic saline solution 2 to 5 mL (injection with a 30x8 needle and drained with the same needle after removal of the syringe. After emptying of the joint, 1mL saline solution will be injected. Patients will ask to answer Visual Analog Scale (VAS) questionnaire, Range of Motion (ROM), Quick DASH, Sollerman Test, and functional grip strength (palmar grip strength, lateral grip strength and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint.
Under sterile conditions, the 1st carpometacarpal (CMC) will be locally anesthetized with ropivacaine and will be submitted to lavage with physiologic saline solution and Osteonil® Mini 1mL of 10mg will be injected in the 1st CMC joint. Patients will ask to answer Visual Analog Scale (VAS) questionnaire, Range of Motion (ROM), Quick DASH, Sollerman Test, and functional grip strength (palmar grip strength, lateral grip strength and pulp-pulp pinch strength) evaluations immediately prior to the procedure and after 1, 3 and 6 months of each joint.