Local Registry for Data Collection of Patients With Achondroplasia / Hypochondroplasia for Epidemiological, Care and Research Studies
Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY
This registry is a observational, single-center study designed to collect clinical data on patients with achondroplasia and hypochondroplasia.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:
• Confirmed diagnosis of achondroplasia/hypochondroplasia
• Patients (and/or Parents legal guardian when required) able to provide informed consent
Locations
Other Locations
Italy
Medical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan
RECRUITING
Milan
Contact Information
Primary
Maria Francesca Bedeschi, MD
mariafrancesca.bedeschi@policlinico.mi.it
+390255032150
Time Frame
Start Date: 2021-09-01
Estimated Completion Date: 2036-12-31
Participants
Target number of participants: 200
Treatments
Achondroplasia
Hypochondroplasia
Related Therapeutic Areas
Sponsors
Leads: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico