New International CTEPH Registry launched

The New International CTEPH Registry has been successfully launched: on the 16th of February, the first patient was included. The registry will last for at least 3 years and will inlcude sites from all over the world. The data collected will improve the knowledge and understanding of this condition, support the further development of diagnosis and treatment guidelines for patients with CTEPH, and contribute to improving patient care in the long-term.

For more information, please see the section on the New International CTEPH Registry.