Recruiting NCT05328050

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

— Observational Achondroplasia Hypochondroplasia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Registry.
Who it may be relevant to: Registry conditions: Achondroplasia, Hypochondroplasia. Basic parameters: No limits · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Italy
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Official title

Local Registry for Data Collection of Patients With Achondroplasia / Hypochondroplasia for Epidemiological, Care and Research Studies

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

Registry of Achondroplasia and Hypochondroplasia Patients [Time frame: 10 years]

Confirmed diagnosis of achondroplasia/hypochondroplasia
Patients (and/or Parents legal guardian when required) able to provide informed consent

Absence of diagnosis of achondroplasia/hypochondroplasia
Patients (and/or Parents legal guardian when required) not able to provide informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Italy · 1 center

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

NCT: NCT05328050 · NaturalhistoryAch2021