NCT05247645 Data Collection of Patients With Rare Bone Diseases
| NCT ID | NCT05247645 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Luca Sangiorgi |
| Condition | Skeletal Dysplasia |
| Study Type | OBSERVATIONAL |
| Enrollment | 1,000 participants |
| Start Date | 2020-10-10 |
| Primary Completion | 2045-10-09 |
Trial Parameters
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Brief Summary
RD-DATA is a retrospective and prospective data collection, finalized for care and research purposes. It is articulated in main sections - strongly related and mutually dependent on each other - corresponding to different data domains: personal information, clinical data, genetic data, genealogical data, surgeries, etc. This approach has been developed to corroborate and integrate data from different sources and evaluating several aspects of the diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate diseases pathophysiology. Due to legal requirements, institutional directives and organizational issues, we are unable to include individuals residing outside Italy in the registry at this time. We are currently engaged in the preparation of a recruitment process for individuals residing outside Italy.
Eligibility Criteria
Inclusion Criteria: * All patients affected by rare diseases with predominantly skeletal involvement Exclusion Criteria: * Any condition unrelated to rare diseases with predominantly skeletal involvement