Clinical Trials in China / NCT05958901
Recruiting
Observational
Pulmonary Hypertension Observational Study
NCT05958901 · tracked via the Priya Life Science China tracker
Condition(s) studied
Pulmonary Hypertension
Investigational drug(s) / intervention(s)
pulmonary hypertension
pulmonary hypertension: The final outcome observed was a diagnosis of pulmonary hypertension.
Study summary
The purpose of this study is to establish the large PH cohort and biological database in China, aiming for precision medicine to optimize diagnosis and treatment choices.
Eligibility
Inclusion Criteria:
* PH group: When the mean pulmonary artery pressure is greater than 25mmHg at rest or greater than 30mmHg during exercise.
* Signed informed consent obtained prior to participations with the ability to comply with protocol and be available for study visits over 5 years.
Exclusion Criteria:
* Acute exacerbation in the past 3 months Having other respiratory diseases with massive lung tissue destruction such as severe bronchiectasis and tuberculosis, etc.
* Serious uncontrolled diseases thoracic or abdominal surgery in the last 3 months.
* Eye surgery in the last three months.
* Retinal detachment myocardial infarction in the last 3 months.
* Admission to hospital for any cardiac condition in the last month.
* Heart rate over 120 beats per minute.
* Antibacterial chemotherapy for tuberculosis pregnant or breast feeding.
Primary outcome measure(s)
- mean pulmonary arterial pressure — 12 months
For an adult at sea level, when the mean pulmonary arterial pressure is greater than 25 mmHg at rest or greater than 30mmHg during exercise.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| The First Affiliated Hospital of Guangzhou Medical University | Guangzhou | Guangdong | Recruiting |
More The First Affiliated Hospital of Guangzhou Medical University trials in China
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05958901 on ClinicalTrials.gov ↗ ← All trials in China