About this trial
CHina Registry for the chAracteristics and Management strategieS of patiEnts With Pulmonary Hypertension Using Targeted Therapy (CHASE Study)
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Sign informed consent;
Between the ages of 18 and 85;
Clinical diagnosis of pulmonary hypertension, using or planning to use pulmonary hypertension targeted drugs (including any one or more of the following: prostacyclin analogues, endothelin receptor antagonists, phosphodiesterase inhibitors, soluble guanylate cyclase agonists and prostacyclin receptor agonists).
Disqualifiers
Have a history of mental illness or drug or poison addiction, and can not sign informed consent or can not cooperate with the experimental study;
Patients with malignant tumor and other diseases and life expectancy of less than half a year;
Short-term (less than 2 weeks) patients taking targeted drugs for pulmonary hypertension
Trial population
Patients with pulmonary hypertension receiving targeted therapy
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Incidence of clinical worsening events 1 year after enrollment
All-cause death, Pulmonary hypertension progression associated with re-hospitalization, Progress of pulmonary hypertension disease
Secondary outcomes
Incidence of all-cause death 1,3,5 year(s) after enrollment
Incidence of all-cause death 1,3,5 year(s) after enrollment
Sponsors and contacts
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