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

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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05328050

Acronym

OMPR-Ach/Hy

Enrollment

200

Registered

2022-04-14

Start date

2021-09-01

Completion date

2036-12-31

Last updated

2022-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Achondroplasia, Hypochondroplasia

Brief summary

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

Interventions

OTHERRegistry

observational, data collection

Study design

Observational model

COHORT

Time perspective

OTHER

Eligibility

Sex/Gender

ALL

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
Registry of Achondroplasia and Hypochondroplasia Patients	10 years	Collection of medical information of achondroplasia and hypochndroplasia patients intended for use in future research studies.

Countries

Italy

Contacts

Primary ContactMaria Francesca Bedeschi, MD

mariafrancesca.bedeschi@policlinico.mi.it+390255032150

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026