Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:39 AM
Ignite Modification Date:
2025-12-25 @ 2:39 AM
NCT ID:
NCT03879434
Eligibility Criteria:
Inclusion Criteria:
* Subjects ≥ 18 years of age and in good general health condition
* Signed informed consent
* Existing Ostenil® Mini recommendation for the treatment of 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)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
99 Years
Study:
NCT03879434
Study Brief:
Protocol Section:
NCT03879434