Data Collection of Patients With Rare Bone Diseases

Launched by LUCA SANGIORGI · Feb 9, 2022

Keywords

ClinConnect Summary

The RD-DATA clinical trial is focused on collecting important information about patients with rare bone diseases, specifically conditions called skeletal dysplasias. This study aims to gather various types of data, such as personal health information, genetic details, and surgical histories, to better understand these diseases. By looking at how genetics might influence the symptoms and outcomes of these conditions, the researchers hope to gain insights that can improve care and treatment for patients.

Anyone with a rare disease that affects the bones may be eligible to participate, regardless of age or gender. However, individuals with conditions unrelated to these rare bone diseases will not be included. Participants in this study can expect to share their medical information, which will be used to help researchers learn more about the diseases. This trial is currently recruiting, and by joining, patients will contribute to important research that may lead to better understanding and management of skeletal dysplasias in the future.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • All patients affected by rare diseases with predominantly skeletal involvement
• Exclusion Criteria:
• • Any condition unrelated to rare diseases with predominantly skeletal involvement