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The study of the intervention with statin on PE and CTEPH

The study of the intervention with statin on PE and CTEPH

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNRC-08000263
Enrollment
Unknown
Registered
2008-12-18
Start date
2008-06-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pulmonary embolism and chronic thromboembolic pulmonary hypertension

Interventions

Group A:basic treatment + atorvastatin
Group B:basic treatment

Sponsors

Tongji Hospital of Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The diagnosis of the PE patients must meet 2 conditions of the followings: (1) Selectivity pulmonary arteriography showes pulmonary artery obstruction or filling defect; (2) Lung ventilation-perfusion scan manifests single or multiple blood perfusion defect, venting normal or unmoral, venting-dabble matchless; (3) Clinical diagnosis: With risk factors for pulmonary embolism and clinical performance, electrocardiogram and chest film exclude other cardiovascular diseases and echocardiography, chest CT, blood gas analysis, D-dimer detection of combining support PTE diagnosis. 2. The diagnosis standard of Chronic Thromboembolic Pulmonary Hypertension (CTEPH) (1)The mean pulmonary artery pressure is >=25mmHg ,while pulmonary capillary wedge pressure(PCWP)is normal (<=15mmHg); (2) Lung ventilation-perfusion scan manifests single or multiple blood perfusion defect, venting normal or unmoral, venting-dabble matchless; (3) Clinical diagnosis: With risk factors for pulmonary embolism or VTE history, clinical exertional dyspnea for more than six months, electrocardiogram and chest film exclude other cardiovascular diseases and echocardiography, chest CT, blood gas analysis, D-dimer detection of combining support PTE diagnosis.

Exclusion criteria

Exclusion criteria: 1. With severe chronic obstructive pulmonary disease: FEV1/FVC<0.5; 2. Low-density lipoprotein cholesterol-C (LDL-C)<70mg/dl; 3. Patient refuse to take part in or can not co-operate the study; 4. With hemorrhagic diseases (such as active peptic ulcer disease, intracranial hemorrhage, trauma or other hemorrhagic diseases); 5. The level of serum transaminase is 3 times more than the normal limit; Or creatine kinase (CK) 5 times more than the normal limit; 6. With other severe heart diseases, as follows: (1) Severe arrhythmia; (2) Unstable Angina; (3) Within six months after myocardial infarction; (4) Cardiac function grade is IV (NYHA classification); (5) Cerebrovascular diseases(such as transient ischemic attack, stroke) or other Cerebral arterial ischemia; (6) Patients who is under 18 or older than 80; (7) Patients with known drug sensitivity or drug allergy; (8) Women who is in gestationperiod or lactation.

Design outcomes

Primary

MeasureTime frame
venous blood biochemical index (including liver enzyme, creatine kinase, etc);1) cardiac and pulmonary function classification; 2) six minute walking distance (6MWD); 3) echocardiograph;

Countries

China

Contacts

Public ContactHaoming Song
songhao-ming@163.com+86 0 13004113931

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026