Registration Study for Rare Type of Pulmonary Hypertension

Status: Recruiting
Location: See location...
Intervention Type: Genetic, Other
Study Type: Observational
SUMMARY

The knowledge on the rare type of pulmonary hypertension which can not be explained by left heart disease, respiratory disease or congenital heart disease is very limited. Investigators aim to setup a national registration study for the rare type of pulmonary hypertension, to understand the natural history, survival, progression, genetic and environmental contributions to disease.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:

• Participant is willing and able to give informed consent for participation in the study.

• Patients diagnosed as idiopathic pulmonary artery hypertension, hereditary pulmonary artery hypertension, hereditary hemorrhagic telangiectasia associated pulmonary artery hypertension, pulmonary veno-occlusive disease, pulmonary capillary hemangiomatosis associated pulmonary artery hypertension, cavernous transformation of portal vein associated pulmonary artery hypertension, special type of congenital heart disease associated pulmonary artery hypertension, chronic thromboembolism pulmonary hypertension.

• All patients should have undergone right heart catheterization, diagnosed according to the guideline.

• Participant is willing and able to give informed consent for participation in the study.

• Self-reported to be healthy

Locations
Other Locations
China
Chinese Academy of Medical Sciences Fuwai Hospital and Peking Union Medical College Hospital
RECRUITING
Beijing
Contact Information
Primary
Xi-Qi XU, MD. PhD.
xuxiqi0928@163.com
+861088322267
Backup
Xin JIANG, MD. PhD.
jxcs983@163.com
+861088396016
Time Frame
Start Date: 2017-05-06
Estimated Completion Date: 2040-12-31
Participants
Target number of participants: 2000
Treatments
Idiopathic Pulmonary Artery Hypertension
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to idiopathic pulmonary artery hypertension (PAH).
Hereditary PAH
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to hereditary PAH.
Hereditary Hemorrhagic Telangiectasia
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to hereditary hemorrhagic telangiectasia associated PAH.
Pulmonary Veno-Occlusive Disease (PVOD)
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to PVOD.
Pulmonary Capillary Hemangiomatosis
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to pulmonary capillary hemangiomatosis associated PAH
Cavernous Transformation of Portal Vein
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to cavernous transformation of portal vein associated PAH
CTEPH
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to chronic thromboembolism pulmonary hypertension (CTEPH).
Pulmonary Takaysu Arteritis
Investigators will conduct laboratory biomarker analysis and genetic analysis to identify pathogenesis or factors related to Pulmonary Takaysu Arteritis.
Sponsors
Collaborators: Peking Union Medical College Hospital
Leads: China National Center for Cardiovascular Diseases

This content was sourced from clinicaltrials.gov