RecruitingNot Applicable

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

Italy200 participantsStarted 2021-09-01

Plain-language summary

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

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Registry of Achondroplasia and Hypochondroplasia Patients

Timeframe: 10 years

Trial details

NCT IDNCT05328050

SponsorFondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2031-12-31

Contact for this trial

Maria Francesca Bedeschi, MD

+390255032150 mariafrancesca.bedeschi@policlinico.mi.it

View on ClinicalTrials.gov More Achondroplasia trials