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Clinical Trial 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.


Clinical Trial Description

The main research contents of this registration study includes: 1. Build a baseline database of the rare type of pulmonary hypertension. Collect general information, on-set symptoms and time, laboratory examination, imaging results, right heart catheterization and treatment information. 2. Follow up recruited patients at regular intervals(6m~1y). Collect information on change in patients condition, laboratory test and treatment. 3. Conduct genetic testing for gene mutation related or hereditary pulmonary hypertension. Link the clinical database to genetic database. 4. Establish bio-bank for serum/plasma, urine, stool, tissues or cells. 5. Establish prognostic study based on the clinical follow-up and genetic database. 6. Draw diagnostic and treatment algorithm for the rare type of pulmonary hypertension. Controls subjects: blood sample and medical data collected once. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03169010
Study type Observational [Patient Registry]
Source China National Center for Cardiovascular Diseases
Contact Xi-Qi XU, MD. PhD.
Phone +861088322267
Email xuxiqi0928@163.com
Status Recruiting
Phase
Start date May 6, 2017
Completion date December 31, 2040

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