This observational study will involve analysis of data collected by the National Rare Disease Registry or medical records .The study will describe outcomes only in PAH(Pulmonary arterial hypertension) patients treated with sildenafil; there will be no comparison with another treatment group. Approximately 100 adults with PAH will be recruited in China hospitals This NIS(non-interventional study) data will be recorded by a physician in the medical records, during the patients' clinical visits, and in the electronic Case Report Forms (CRF).
Study Type
OBSERVATIONAL
Enrollment
100
Participants need to take the Revatio as per Physician's prescription
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
Guangdong Provincial People's Hospital
Guangdong, Guangzhou, China
The Second Xiangya Hospital Of Central South University
Changsha, Hunan, China
The First Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, China
Affiliated Hospital of Jining Medical College
Jining, Shandong, China
Tianjin Medical University General Hospital
Tianjin, Tianjin Municipality, China
Yanan Hospital of Kunming City
Kunming, Yunnan, China
Treatment-emergent Adverse Events (TEAEs)
Incidence of TEAEs and the type of TEAEs
Time frame: From baseline to week24
Serious adverse events (SAEs)
Incidence of SAE and the type of SAE
Time frame: From baseline to week24
6-MWD (6-minute walk distance)
Change in 6-minute walk distance (6-MWD)
Time frame: baseline, week 12, week24
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