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Chondroitin Sulphate Treatment Efficacy in Rhizarthrosis. Measurement With Sensory and Quantitive Functional Tests and Concordance Analysis With Subjective Scales of Pain.
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.
Age
45 - 75 years
Sex
ALL
Healthy Volunteers
No
Hospital Clínic i Provincial de Barcelona
Barcelona, Catalonia, Spain
Start Date
March 1, 2011
Primary Completion Date
April 1, 2013
Completion Date
April 1, 2013
Last Updated
February 22, 2013
108
ESTIMATED participants
Chondroitin sulfate
DRUG
Placebo
DRUG
Lead Sponsor
Juan A. Arnaiz
NCT06858800
NCT05915962
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.
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View ClinicalTrials.gov Terms and ConditionsNCT04588961