This is an open-label, uncontrolled, prospective long-term observation of Specific Drug in the treatment of patients with pulmonary hypertension up to 4 years. 160 patients with primary (idiopathic and familial) pulmonary hypertension (PH) or pulmonary arterial hypertension (PAH) due to scleroderma with New York Heart Association (NYHA) functional class and exercise capacity, defined as class III and IV planned to enroll. Efficacy, safety and tolerability of the drug and the survival of the patients will be observed.
Study Type
OBSERVATIONAL
Enrollment
118
Since this study is an observational, inhaled iloprost dosage and frequency for each patient will be prescribed by physicians as medically required.
Unnamed facility
Multiple Locations, Turkey (Türkiye)
6 Minutes walking distance (change in meters)
Time frame: At month 48
Adverse events, weight, vital findings
Time frame: At month 48
6 Minutes walking distance (% change)
Time frame: At month 48
New York Heart Association Functional Class
Time frame: At month 48
Change in drug dosage or frequency, need for PAH specific drug combination, need for drug change
Time frame: At month 48
Pulmonary hypertension related hospitalization
Time frame: At month 48
Heart and/or lung transplantation, mortality
Time frame: At month 48
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