Registry of patients with pulmonary hypertension receiving targeted therapy
Official title: CHina Registry for the chAracteristics and Management strategieS of patiEnts With Pulmonary Hypertension Using Targeted Therapy
Run by Chinese Pulmonary Vascular Disease Research Group · NCT06135909 · Data updated 2026-11-12
This study is collecting information from over 5,000 patients in China with pulmonary hypertension who are using targeted therapies to see how well these treatments work and how the disease progresses over three years.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 85 Years |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Chinese Pulmonary Vascular Disease Research Group Academic / other |
| Locations | 1 site (Beijing) |
| Status | Recruiting |
| Started | January 1, 2020 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | January 18, 2024 |
| Trial ID | NCT06135909 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals aged 18 to 85 with a clinical diagnosis of pulmonary hypertension who are currently using or planning to use targeted therapies.
✕Probably not a fit
Patients with a history of mental illness, drug addiction, or those with a life expectancy of less than six months due to other diseases may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The CHASE Registry aims to collect and analyze clinical characteristics and treatment strategies of patients with pulmonary hypertension in China who are receiving targeted therapies. This multicenter, prospective observational study will enroll at least 5000 patients, who will be followed for three years with assessments every six months. The study focuses on real-world data to understand disease progression, treatment outcomes, and the effectiveness of targeted drugs in managing pulmonary hypertension.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the management and treatment outcomes of pulmonary hypertension, potentially improving patient care.
How similar studies have gone: Other studies focusing on real-world data collection in pulmonary hypertension have shown promise, indicating that this approach may yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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). Exclusion Criteria: * 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
Where it's running
-
Center for Respiratory and Pulmonary Vascular Diseases, Fuwai hospital, CAMS & PUMC
Beijing, China Recruiting
Study contacts
- Principal investigator: Zhihong Liu, M.D., Ph.D — Chinese Academy of Medical Sciences, Fuwai Hospital
- Study coordinator: Zhihong Liu, M.D., Ph.D
- Email: zhihongliufuwai@163.com
- Phone: 8601088396816
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.