Registry of Multiple Osteochondromas That Collects Clinical, Functional, Genetic, Genealogical, Imaging, Surgical, Quality of Life Data. Data Are Linked to Patients Biological Sample
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
REM is a retrospective and prospective registry, finalized to care and research. 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 individuated in order to corroborate and integrate data from different resources and aspects of the diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate diseases pathophysiology.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:
• All Multiple Osteochondromas patients, including prenatal diagnosis of Multiple Osteochondromas
Locations
Other Locations
Italy
Irccs Istituto Ortopedico Rizzoli
RECRUITING
Bologna
Contact Information
Primary
Marina Mordenti, PhD
marina.mordenti@ior.it
+39 05 6366062
Backup
Manila Boarini, MSc
manila.boarini@ior.it
+39 05 6366062
Time Frame
Start Date: 2013-06-28
Estimated Completion Date: 2032-12
Participants
Target number of participants: 10000
Treatments
Multiple Osteochondromas patients
Patients affected by Multiple Osteochondromas. The Registry will include also data on foetuses (prenatal).
Related Therapeutic Areas
Sponsors
Leads: Luca Sangiorgi