Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Data Collection of Patients With Rare Bone Diseases

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.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: Luca SangiorgiUpdated: Nov 20, 2025Locations: 1
Eligibility criteria

All patients affected by rare diseases with predominantly skeletal involvement

Any condition unrelated to rare diseases with predominantly skeletal involvement

Status: Recruiting

Registry of Ollier Disease and Maffucci Syndrome

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.

Participants needed: 400
Trial details
Biological sex: AllType: ObservationalSponsor: Luca SangiorgiUpdated: Nov 20, 2025Locations: 1Duration: 25 Years
Eligibility criteria

All patients affected by Ollier Disease and Maffucci Syndrome

Any condition unrelated to Ollier Disease and/or Maffucci Syndrome

Status: Recruiting

Registry of Multiple Osteochondromas

REM is a retrospective and prospective registry, 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 evaluating several aspects of diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate disease 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.

Participants needed: 10,000
Trial details
Biological sex: AllType: ObservationalSponsor: Luca SangiorgiUpdated: Nov 20, 2025Locations: 1Duration: 25 Years
Eligibility criteria

All Multiple Osteochondromas patients, including prenatal diagnosis of Multiple...

Any condition unrelated to Multiple Osteochondromas

Status: Recruiting

Registry of Ehlers-Danlos Syndrome

RED is a retrospective and prospective registry, 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 diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate disease 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.

Participants needed: 3,000
Trial details
Biological sex: AllType: ObservationalSponsor: Luca SangiorgiUpdated: Nov 20, 2025Locations: 1Duration: 25 Years
Eligibility criteria

All Ehlers-Danlos Syndrome patients, including prenatal and fetal diagnosis of E...

Any condition unrelated to Ehlers-Danlos Syndrome

Status: Recruiting

Registry of Osteogenesis Imperfecta

ROI is a retrospective and prospective registry, 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 evaluating several aspects of 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.

Participants needed: 5,000
Trial details
Biological sex: AllType: ObservationalSponsor: Luca SangiorgiUpdated: Nov 20, 2025Locations: 1Duration: 25 Years
Eligibility criteria

All Osteogenesis Imperfecta patients, including prenatal and fetal diagnosis of...

Any condition unrelated to Osteogenesis Imperfecta