Influence of the Radiological Stage on the Efficiency of Viscosupplementation in Basal Thumb Arthritis
Launched by LABRHA · Aug 7, 2018
Trial Information
Current as of June 30, 2025
Completed
Keywords
ClinConnect Summary
Fifty patients presenting a rhizarthrose asserted by radiography and justifying a viscosupplement, without other selection criterion than the opinion of the investigator concerning the legitimacy of a viscosupplement and the agreement of the patient participating in the study.
The patients are identified by N ° of center (01 - 10) followed by the inclusion order number for every center (from 1 to 10).
The informations collected during the initial consultation (J0) are: demographic (sex, age, weight, size), pathological (history of the disease, bilaterality, prosthesis of thumb contralater...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients of both genders, of all ages
- • Rhizarthrosis confirmed by radiography including frontal and KAPANDJI side radiographies performed during the last 6 months
- • Patients requiring a viscosupplement based on the opinion of the investigator
- • Patients were able to read and understand the information sheet, to give their enlighted consent and to respect follow up consultations
- Exclusion Criteria:
- • Patient with hypersensitivity to hyaluronic acid or mannitol
- • Patient with a contraindication to the injection procedure : infected skin lesions on or close to an injection site, infectious disease ongoing
- • Patient who received a viscosuplement during the last 3 months
- • Patient who received an intra-articular injection of corticoids in the target articulation during the month before the inclusion
- • Patient not talking french
About Labrha
Labrha is a pioneering clinical trial sponsor dedicated to advancing medical research and innovation through the development of cutting-edge therapies. With a focus on enhancing patient outcomes, Labrha specializes in designing and conducting Phase I to IV clinical trials across a diverse range of therapeutic areas. Leveraging a team of experienced professionals and state-of-the-art technology, Labrha is committed to ensuring rigorous compliance with regulatory standards while fostering collaboration with healthcare providers and research institutions. Their mission is to accelerate the delivery of safe and effective treatments to patients worldwide, ultimately contributing to the advancement of global health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lyon, , France
Patients applied
Trial Officials
thierry CONROZIER, MD
Principal Investigator
Labrha
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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