Registry for Patients With Achondroplasia / Hypochondroplasia (OMPR-Ach/Hy)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorFondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
About this trial
This registry is a observational, single-center study designed to collect clinical data on patients with achondroplasia and hypochondroplasia.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Confirmed diagnosis of achondroplasia/hypochondroplasia
Patients (and/or Parents legal guardian when required) able to provide informed consent
Disqualifiers
Absence of diagnosis of achondroplasia/hypochondroplasia
Patients (and/or Parents legal guardian when required) not able to provide informed consent
Trial population
Patients With Achondroplasia / Hypochondroplasia afferent to IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano
Trial design
Design model
Cohort
Time perspective
Other
Treatments tested in this trial
Registry
Other interventionobservational, data collection
Treatment groups
200 Participants
are divided into 2 treatment groupsGroup A: Achondroplasia1 intervention
Group B: Hypochondroplasia1 intervention
Trial outcomes
Primary outcomes
1
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 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov