Routine Application of Ostenil® Mini in Patients with Rhizarthrosis

Exclusion Criteria

• •Known hypersensitivity to one of the Ostenil® Mini components
• •Known pregnancy or lactating females
• •Presence of coagulation disorder
• •Subjects not capable of contracting and of understanding the nature, risks, significance and implications of the clinical investigation and unable to form a rational intention in the light of these facts
• •Subjects unable to understand informed consent or having a high probability of non compliance to the study procedures and / or non completion of the study according to investigator's judgement (e.g. illiteracy, insufficient knowledge of local language)