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Clinical Trials/NCT05328050
NCT05328050
Recruiting
N/A

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

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico1 site in 1 country200 target enrollmentSeptember 1, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Achondroplasia
Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Enrollment
200
Locations
1
Primary Endpoint
Registry of Achondroplasia and Hypochondroplasia Patients
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
December 31, 2036
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maria Francesca Bedeschi

Principal investigator

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Eligibility Criteria

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

Outcomes

Primary Outcomes

Registry of Achondroplasia and Hypochondroplasia Patients

Time Frame: 10 years

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

Study Sites (1)

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