CHASE Registry of Patients With Pulmonary Hypertension Receiving Targeted Therapy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorChinese Pulmonary Vascular Disease Research Group

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

5,000 Participants
are grouped into 1 trial group
Group A: PH Patients receiving targeted drugs treatment

Trial outcomes

Primary outcomes

1

Incidence of clinical worsening events 1 year after enrollment

All-cause death, Pulmonary hypertension progression associated with re-hospitalization, Progress of pulmonary hypertension disease

Time frame
1 year after enrollment

Secondary outcomes

1

Incidence of all-cause death 1,3,5 year(s) after enrollment

Incidence of all-cause death 1,3,5 year(s) after enrollment

Time frame
1,3,5 year(s) after enrollment

Other outcomes

Sponsors and contacts

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