Pre-Pulmonary Atrial Hypertension
Conditions
Keywords
Pre-Pulmonary Atrial Hypertension
Brief summary
This research study is looking at the use of the drug ambrisentan and if it can improve right ventricle function in people with systemic sclerosis-associated pre-pulmonary arterial hypertension. It is also looking at using right ventricle function changes as a marker of disease severity.
Detailed description
This research study is looking at the use of the drug ambrisentan and if it can improve right ventricle function in people with systemic sclerosis-associated pre-pulmonary arterial hypertension. It is also looking at using right ventricle function changes as a marker of disease severity. Pre-pulmonary arterial hypertension is a borderline elevation in blood pressure in the lungs. Pre-pulmonary arterial hypertension is not currently treated with the drug therapies that are used for pulmonary arterial hypertension. It represents a group of patients that are at risk for developing pulmonary arterial hypertension. The administration of ambrisentan is the experimental part of this study. Ambrisentan has not been approved by the FDA for use of improving right ventricle function in people with pre-pulmonary arterial hypertension. You will still receive your normal clinical care. The purpose of this study is to learn more about ambrisentan and its role in treating systemic sclerosis-associated pre-pulmonary arterial hypertension. Ambrisentan is already approved for use in people with systemic sclerosis-associated pulmonary arterial hypertension, but this study wants to research its role in people with pre-pulmonary arterial hypertension.
Interventions
DRUGAmbrisentan
Subjects will be randomized 1:1 ratio according to computer generated random numbers to receive either placebo or ambrisentan 5mg daily for one month followed by 10 mg daily for the 5 months in a double-blinded manner.
Sponsors
National Jewish Health
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Age \>18 years, \< 80 years * Systemic sclerosis with any of the following features: 1. Duration of Raynaud's phenomena \>8 years 2. Anticentromere antibody positivity 3. isolated nucleolar-pattern ANA positivity 4. Extensive telangiectasias 5. DLCO \< 60% in the absence of extensive ILD 6. FVC%/DLCO% \>1.6 7. Unexplained dyspnea * Right heart catheterization-proven pre PAH (mean PAP 20-25 mmHg and pulmonary capillary wedge pressure \<15 mmHg) * Systolic blood pressure \>100 mmHg * Reliable contraception for women of childbearing age * Informed consent
Exclusion criteria
* \< 18 years or \> 80 years * Left ventricular ejection fraction \< 55% * Systolic or diastolic left ventricular congestive heart failure * Liver disease (abnormal AST/ALT, chronic hepatitis, or cirrhosis) * Extensive ILD or FVC\< 60% * Pregnant * Breast-feeding women * Cyclosporine use
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in right ventricular (RV) myocardio strain > 2% | 1, 3 and 6 months | Assess for tolerance, gas exchange, and therapeutic benefit, resting oximetry, six minute walk with oximetry, pulmonary function testing with diffusion capacity (DLCO), and functional class will be assessed prior to ambrisentan initiation, and 1,3, and 6 months. |
Countries
United States
Outcome results
None listed