Safety Surveillance of Targeted Drugs for Pulmonary Hypertension Using a Computerized Follow-up System: a Nationwide Cohort Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Recruit at least 700 PH patients, follow up every 6 months based on a computerized follow-up system. Primary outcomes are adverse drug events and all-cause death.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3 months
Maximum Age: 85
Healthy Volunteers: f
View:

• Age from 3 months to 85 years, no sex preference;

• Right heart catheter meet the following conditions simultaneously: mPAP≥25mmHg, and PVR \> 3 Wood units(in children PVRi \> 3 WU x m2), and PAWP≤15 mmHg at rest;

• Patients diagnosed with group 1,2,4,5 PH according to the WHO classification, detailed description is as follows: Pulmonary arterial hypertension, Lung disease / chronic hypoxia associated pulmonary hypertension, Pulmonary hypertension associated with pulmonary artery stenosis / obstruction and Pulmonary hypertension caused by other multiple factors

• Take at least one pulmonary hypertension targeted drug or calcium antagonist;

• Signed written informed consent.

Locations
Other Locations
China
Fuwai Hospital, Chinese Academy of Medical Sciences
RECRUITING
Beijing
Contact Information
Primary
Tingting Guo, M.D
18610094559@163.com
+86 18610094559
Time Frame
Start Date: 2021-08-26
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 700
Related Therapeutic Areas
Sponsors
Leads: China National Center for Cardiovascular Diseases

This content was sourced from clinicaltrials.gov