Physiopathology of Pulmonary Arterial Hypertension: Mechanistic Studies

NCT02959723 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2016-11-09

No results posted yet for this study

Summary

The current aims to combine analysis of different inflammatory biomarkers and BMPR2 mutations, which are currently analyzed in each patient diagnosed with idiopathic or familial PAH, to establish an earlier diagnosis and consequently better orientate the therapeutic strategy in PAH.

Conditions

  • Idiopathic Pulmonary Arterial Hypertension

Sponsors & Collaborators

  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Eligibility

Min Age
15 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2017-12-31
Completion
2020-12-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02959723 on ClinicalTrials.gov