Patients who present rhizarthrosis diagnostic will be randomized to be treated with chondroitin sulfate or placebo during 24 weeks to study the effect of the treatment with objective and subjective indicators of pain and sensibility.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
108
Administration of 2 capsules of 400 mg of chondroitin sulfate orally.
Administration of 2 capsules of placebo orally.
Hospital Clínic i Provincial de Barcelona
Barcelona, Catalonia, Spain
RECRUITINGEvaluation with visual analogue pain scale as mean at the last weak
Time frame: 36 weeks
Sollerman test
Evaluation of hand function with Sollerman test
Time frame: 36 weeks
Hand pressure force
Time frame: 36 weeks
Thumb-index finger pincer force
Time frame: 36 weeks
Dash test
Osteoarthritis functional test
Time frame: 36 weeks
SF-12 test
Quality of life test
Time frame: 36 weeks
Mechanical sensitivity measured with electronic Von Frey filament
Time frame: 36 weeks
vibratory and thermic sensibility threshold assisted by computer
Time frame: 36 weeks
Use of paracetamol or other analgesic drugs
recorded in a patient diary
Time frame: 36 weeks
Evolution of trapezium-thumb metacarpal joint by ultrasound scan
Time frame: 36 weeks
Hematologic evaluation
Time frame: 24 weeks
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Biochemical evaluation
Time frame: 24 weeks