Trans-pulmonary Biomarkers in Pulmonary Hypertension
Running, not enrolling
Conditions studied: Pulmonary Hypertension
In brief
The investigators are testing whether the addition of Pulmonary Hypertension-related biomarkers, measured across the pulmonary circulation, to the standard hemodynamic evaluation for Pulmonary Hypertension will lead to more informed choices of Pulmonary Hypertension therapy and improved patient outcomes.
Key facts
- Study ID
- NCT01961232
- Run by
- Vanderbilt University
- People needed
- 100
- Starts
- 2013-08-01
- Expected to finish
- 2027-06-01
- Last updated by the study team
- 2026-03-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years old
- Undergoing RHC for PH evaluation
You may not qualify if…
- Anemia defined as Hgb < 10 g/dL and HCT < 30
- Pregnancy at the time of RHC (as assessed by urine or serum pregnancy test on the day of the procedure)
- Left ventricular ejection fraction ≤ 40%
- Atrial fibrillation at the time of RHC (as defined by telemetry monitoring or EKG on the day of the procedure)
- IPF, CTEPH, COPD/OSA as the dominant etiology of PH
- Patient is currently taking PH medication or long-acting nitrates at the time of their RHC.
Where it is running
- Vanderbilt University Medical Center — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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