Registry of Ollier Disease and Maffucci Syndrome 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 patients affected by Ollier Disease and Maffucci Syndrome

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: 2017-01-16
Estimated Completion Date: 2032-01
Participants
Target number of participants: 400
Treatments
Ollier Disease and Maffucci Syndrome patients
The group comprises all patients affected by Ollier Disease and Maffucci Syndrome.
Related Therapeutic Areas
Sponsors
Leads: Luca Sangiorgi

This content was sourced from clinicaltrials.gov