Registry for Patients With Achondroplasia / Hypochondroplasia (OMPR-Ach/Hy)

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico200 enrolled

Overview

This registry is a observational, single-center study designed to collect clinical data on patients with achondroplasia and hypochondroplasia.

Study Type

OBSERVATIONAL

Enrollment

200

Conditions

Achondroplasia Hypochondroplasia

Interventions

RegistryOTHER

observational, data collection

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Confirmed diagnosis of achondroplasia/hypochondroplasia * Patients (and/or Parents legal guardian when required) able to provide informed consent Exclusion Criteria: * Absence of diagnosis of achondroplasia/hypochondroplasia * Patients (and/or Parents legal guardian when required) not able to provide informed consent

Locations (1)

Medical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan

Milan, Italy

RECRUITING

Outcomes

Primary Outcomes

Registry of Achondroplasia and Hypochondroplasia Patients

Collection of medical information of achondroplasia and hypochndroplasia patients intended for use in future research studies.

Time frame: 10 years

Central Contacts

Maria Francesca Bedeschi, MD

CONTACT

+390255032150 mariafrancesca.bedeschi@policlinico.mi.it

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.