I27.0 I27.28
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: confirmed pulmonary hypertension with mPAP >19 mmHg and PAWP <16 mmHg; WHO functionall class incuding IPAH, HPAH, APAH; no change in therapy for 6 weeks; increades fluid intake (<2l/d) and/or signs of fluid overload and/or multiple decompensations in the past
Exclusion criteria
Exclusion criteria: underaged patients; no confirmed pulmonary hypertension; WHO group II-V; LVEF <50%; pulmonary disease defined as FEV1 <50% and/or TLC <70%; pregnancy/nursing period; not suitable for other medical reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| change of the right atrial area; change of the right ventricular area both parameters from baseline to 24 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| weight, oedema, cardiac biomarkers, quality of life, quantity of hospitalizations, clinical outcome, Compliance, subjective parameters Baseline to week 12 and week 24 | — |
Countries
Germany