Registry of Ollier Disease and Maffucci Syndrome
Recruiting now
Conditions studied: Ollier Disease, Maffucci Syndrome
In brief
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. 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.
Key facts
- Study ID
- NCT04134572
- Run by
- Luca Sangiorgi
- People needed
- 400
- Starts
- 2017-01-16
- Expected to finish
- 2032-01-01
- Last updated by the study team
- 2025-11-20
Who can join
Age: any. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- All patients affected by Ollier Disease and Maffucci Syndrome
You may not qualify if…
- Any condition unrelated to Ollier Disease and/or Maffucci Syndrome
Where it is running
- Irccs Istituto Ortopedico Rizzoli — Bologna, Emilia-Romagna, Italy (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.