Registry and biobank for adults with pulmonary hypertension

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study involves creating a prospective registry and biobank for adult patients diagnosed with various groups of pulmonary hypertension. Participants will be enrolled and their body fluid samples will be collected at the start and during treatment with targeted therapies. The aim is to gather long-term observational data to better understand the condition and its treatment outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Diagnosis of pulmonary hypertension group 1 to 5
* Ability to give informed consent

Exclusion Criteria:

\- Withdrawal of informed consent

Where it's running

• Universitätsklinikum Hamburg-Eppendorf
  Hamburg, Free and Hanseatic City of Hamburg, Germany Recruiting

Study contacts

• Study coordinator: Lars Harbaum, MD
• Email: l.harbaum@uke.de
• Phone: +4940741018337

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.