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

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

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Phase N/A
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  • Simplified (AI rewritten)

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Overview

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

Eligibility

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

Study details
    Achondroplasia
    Hypochondroplasia

NCT05328050

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

26 January 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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