CHASE Registry of Patients With Pulmonary Hypertension Receiving Targeted Therapy

Last updated: January 16, 2024
Sponsor: Chinese Pulmonary Vascular Disease Research Group
Overall Status: Active - Recruiting

Phase

N/A

Condition

Congestive Heart Failure

Scleroderma

High Blood Pressure (Hypertension)

Treatment

N/A

Clinical Study ID

NCT06135909
CHASE
  • Ages 18-85
  • All Genders

Study Summary

CHina Registry for the chAracteristics and Management strategieS of patiEnts With Pulmonary Hypertension Using Targeted Therapy (CHASE Study)

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Sign informed consent;
  • Between the ages of 18 and 85;
  • Clinical diagnosis of pulmonary hypertension, using or planning to use pulmonaryhypertension targeted drugs (including any one or more of the following: prostacyclinanalogues, endothelin receptor antagonists, phosphodiesterase inhibitors, solubleguanylate cyclase agonists and prostacyclin receptor agonists).

Exclusion

Exclusion Criteria:

  • Have a history of mental illness or drug or poison addiction, and can not signinformed consent or can not cooperate with the experimental study;
  • Patients with malignant tumor and other diseases and life expectancy of less than halfa year;
  • Short-term (less than 2 weeks) patients taking targeted drugs for pulmonaryhypertension

Study Design

Total Participants: 5000
Study Start date:
January 01, 2020
Estimated Completion Date:
December 31, 2027

Study Description

The purpose of this study was to establish the clinical characteristics and treatment strategies of targeted pulmonary hypertension patients in China: a multicenter, prospective case registry (CHASE) study to describe the clinical characteristics, treatment used, disease progression, and outcomes (e.g., death, hospitalization) of patients taking targeted drugs in real-world clinical practice. This study will collect high-quality real-world data that can be used as a standalone dataset or combined with other data sources to address critical issues in the PH field.

This is a prospective, observational, multicenter study. The expected number of enrolled cases for the entire study: at least 5000; No experimental group and control group were divided. Patients were followed up every 6 months ±2 weeks after enrollment for 3 years. The study selected patients who signed informed consent, aged 18-25 years, clinically diagnosed with pulmonary hypertension, and were applying or planning to apply targeted drugs for pulmonary hypertension as the study objects. The primary endpoint was the incidence of clinical exacerbations at 1 year after enrollment. Secondary endpoints were all-cause mortality at 1, 2, and 3 years after enrollment, rate of lung transplantation or combined cardiopulmonary transplantation, 6-minute walking distance, NT-proBNP level, WHO cardiac function grade, ratio of right ventricular end-diastolic diameter to left ventricular end-diastolic diameter, pulmonary hypertension targeted drug regimen, and incidence of associated adverse reactions.

Connect with a study center

  • Center for Respiratory and Pulmonary Vascular Diseases, Fuwai hospital, CAMS & PUMC

    Beijing, 100037
    China

    Active - Recruiting

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