Acute Coronary Syndrome, Coronary Artery Bypass Graft, Percutaneous Coronary Artery Intervention
Conditions
Keywords
percutaneous coronary artery intervention, coronary artery bypass graft, acute coronary syndrome
Brief summary
The purpose of this study is to built the standard of Chinese Traditional Medicine test for Post percutaneous coronary artery intervention and coronary artery bypass graft，also for acute coronary syndrome，according to the multi-site、random large sample test.
Interventions
DRUGcipher prescription 1
Drug granules include ginseng,RADIX NOTOGINSENG,prepared RHIZOMA PINELLIAE with alumen radix glyrrhigae calcaren once daily for 180 days
DRUGcipher prescription 2
Placebo include amidon、bitter principles and diluents bases once daily for 180 days
Sponsors
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Guangdong Provincial People's Hospital
China-Japan Friendship Hospital
Traditional Chinese Medicine Hospital of Xinjiang Uygur Autonomous Region
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Teaching Hospital of Nanjin University of Traditional Chinese Medicine
Second People's Hospital, Fujian Province
Liaoning University of Traditional Chinese Medicine
Guangzhou Overseas Chinese Hospital
Beijing Tongren Hospital
Shanghai 10th People's Hospital
PLA.The Military General Hospital of Beijing
The Sixth Affliated Hospital of Jinan University
Beijing Anzhen Hospital
Gansu Provincial Hospital
Shaanxi Provincial People's Hospital
First Affiliated Hospital, Sun Yat-Sen University
The Fifth Affliated Hospital of Guangxi Medical University
Guangzhou University of Chinese Medicine
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* age40～75 * angina or CAD patient * deficiency of heart-QI and blockage of phlegm and blood stasis in chinese medicine * 1 week after operation，or 1week after drainage tube extraction for CABG * sign a informed consent
Exclusion criteria
* severe cardia failure * severe renal inadequacy * complicating with malignant tumor,reactive alimentary tract hemorrhage and haematological systemic disorder etc. * psychotic * pregnant,lactation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| dead | 180±3days |
Secondary
| Measure | Time frame |
|---|---|
| cardiovascular event | 180±3days |
Outcome results
None listed