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The Secondary Prevention Trial for Ischemic Stroke With DengzhanShengmai Capsule

Model Study on the Comprehensive Treating Protocol and Effect Evaluation of Ischemic Stroke With Traditional Chinese Medicine

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00548223
Acronym
SPIRITDZSM1
Enrollment
3143
Registered
2007-10-23
Start date
2007-12-31
Completion date
2011-01-31
Last updated
2013-08-07

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

Conditions

Stroke

Keywords

recurrence of stroke, Dengzhan Shengmai Capsule, Traditional Chinese Medicine

Brief summary

In order to observe the secondary preventive effect of the Dengzhanshengmai capsule on ischemic stroke, the investigators hold the large randomized control trial (RCT). 3143 subjects are included in 83 clinical research centers all over China. The subjects are randomly grouped into two groups. The basic therapy included antiplatelet aggregation, stroke health education, management of blood pressure, blood lipid and blood glucose, etc. The treating group will take the compound Chinese Medicine Deng Zhan Sheng Mai capsule and the contrast group will take the placebo for twelve months. Then all of the subjects are visited on the 30th, 90th, 180th, 360th day after inclusion. The recurrence of stroke, cardiovascular events, and peripheral arterial events are observed.

Detailed description

Objective:To observe the secondary clinical effect of the Deng Zhan Sheng Mai capsule on ischemic stroke patients. Methods:3143 subjects suffering from acute ischemic stroke are included in 83 clinical research centers all over China. The subjects are randomly divided into two groups:The treating group and the placebo group.Both groups accept the basic therapy and test drug.The basic therapy included antiplatelet aggregation,stroke health education,management of blood pressure,blood lipid and blood glucose,etc.The patients in Dengzhan Shengmaigroup take Deng Zhan Sheng Mai capsule and the placebo group take the placebo drug for twelve months.Then all of the subjects are visited on the 30th,90th,180th,360th day after inclusion. Primary endpoints(cerebral infarction,intracerebral hemorrhage,subarachnoid hemorrhage) and secondary endpoints(cardiovascular events,peripheral arterial disease),functional disability are observed at each follow up.

Interventions

DRUGDengzhan Shengmai capsule

Capsule, 0.18g, 2#, Bid\*1year

DRUGplacebo

Capsule, 0.18g, 2#, Bid\*1year

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
CollaboratorOTHER
Nanhai Hospital of Traditional Chinese Medicine
CollaboratorOTHER
People's hospital of Huizhou city
CollaboratorUNKNOWN
Taishan city hospital of TCM
CollaboratorUNKNOWN
Ruijin Hospital
CollaboratorOTHER
First Affiliated Hospital of Fujian Medical University
CollaboratorOTHER
Yangjiang City Hospital of TCM in Guangdong Province
CollaboratorUNKNOWN
Xinxing county hospital of TCM
CollaboratorUNKNOWN
Southern branch of yuexiu district hospital of TCM
CollaboratorUNKNOWN
Xinhui hospital of TCM of Jiangmen
CollaboratorUNKNOWN
Shanghai Pudong New Area People's Hospital
CollaboratorOTHER
People's hospital of Jianyang city
CollaboratorUNKNOWN
Luzhou Medical College
CollaboratorOTHER
Mianyang city hospital of TCM
CollaboratorUNKNOWN
Guangyuan city hospital of TCM of Sichuan Province
CollaboratorUNKNOWN
The Third Affiliated Hospital of Guangzhou Medical University
CollaboratorOTHER
Shunde district hospital of TCM
CollaboratorUNKNOWN
Shenzhen People's Hospital
CollaboratorOTHER
Anyue County Hospital of Traditional Chinese
CollaboratorOTHER
Chengdu Integrated TCM&Western Medicine Hospital
CollaboratorUNKNOWN
Guangzhou Red Cross Hospital
CollaboratorOTHER
Jiangsu Provincial People's Hospital
CollaboratorOTHER
Ankang Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Qishan county hospital of shaanxi province
CollaboratorUNKNOWN
Zongrui Hospital
CollaboratorOTHER
First Affiliated Hospital of Xinjiang Medical University
CollaboratorOTHER
Lianyungang Chinese Medicine Hospital
CollaboratorUNKNOWN
Yufu City Hospital of TCM in Guangdong Province
CollaboratorUNKNOWN
169 Military Hospital of China
CollaboratorOTHER
Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
CollaboratorOTHER
The second affiliated hospital of shanxi college of TCM
CollaboratorUNKNOWN
URUMQI Hospital of Traditional Chinese Medicine
CollaboratorUNKNOWN
Hubei General Hospital
CollaboratorUNKNOWN
The People's Hospital of Leshan
CollaboratorOTHER
Guagnzhou Liwan district Hospital of TCM
CollaboratorUNKNOWN
Longhua Hospital
CollaboratorOTHER
Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Hangzhou City Hospital of TCM
CollaboratorUNKNOWN
Dongguan city hospital of TCM
CollaboratorUNKNOWN
Liuzhou City hospital of TCM
CollaboratorUNKNOWN
Maoming city hospital of TCM
CollaboratorUNKNOWN
Beijing Tiantan Hospital
CollaboratorOTHER
Affiliated Hospital of Nantong University
CollaboratorOTHER
Xi'an city hospital of TCM
CollaboratorUNKNOWN
Jiangsu province hospital of TCM
CollaboratorUNKNOWN
The Third People's Hospital of Chengdu
CollaboratorOTHER
Huizhou Municipal Central Hospital
CollaboratorOTHER
Zhejiang Provincial Hospital of TCM
CollaboratorOTHER
The Second People's Hospital of Yibin
CollaboratorOTHER
Shanxi Provincial People's Hospital
CollaboratorOTHER_GOV
The First Affiliated Hospital of Guangzhou Medical University
CollaboratorOTHER
Guangxi Ruikang Hospital
CollaboratorOTHER
Third Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
CollaboratorOTHER
Affiliated Hospital of North Sichuan Medical College
CollaboratorOTHER
Third Affiliated Hospital of Henan University of Traditional Chinese Medicine
CollaboratorOTHER
ZhuHai Hospital
CollaboratorOTHER
Nanfang Hospital, Southern Medical University
CollaboratorOTHER
West China Hospital
CollaboratorOTHER
Guangdong Second Provincial Traditional Chinese Medicine Hospital
CollaboratorINDUSTRY
Handan First Hospital
CollaboratorOTHER
The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
CollaboratorOTHER
Conghua city hospital of TCM
CollaboratorUNKNOWN
The First Affiliated Hospital of Guangxi University of Chinese Medicine
CollaboratorUNKNOWN
Hubei Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Jinan city hospital of TCM
CollaboratorUNKNOWN
Shaanxi Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Suining People's Hospital
CollaboratorUNKNOWN
Wuzhou Red Cross Hospital
CollaboratorOTHER
Wuhan Interated &Western Hospital
CollaboratorUNKNOWN
Second Affiliated Hospital of Xi'an Jiaotong University
CollaboratorOTHER
Xi'an Central Hospital
CollaboratorOTHER
Zhengzhou City Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Xiangya Hospital of Central South University
CollaboratorOTHER
Second Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
The First Affiliated Hospital of Henan University of Traditional Chinese Medicine
CollaboratorOTHER
ShuGuang Hospital
CollaboratorOTHER
Zhongshan Hospital Of Traditional Chinese Medicine
CollaboratorOTHER
Foshan Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Teaching Hospital of Chengdu University of TCM
CollaboratorUNKNOWN
Jiangmen Wuyi Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Guangdong Provincial Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Guangzhou University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* 40-75 years old * Ischemic stroke diagnosed by CT/MRI scan * Patient presenting from 14 days to 6 months of first onset of ischemic stroke * Presence of at least one risk factor of stroke (such as hypertension, diabetes mellitus, coronary heart disease, hyperlipidemia, and smoking, etc.) that can be interfered in * Informed consent

Exclusion criteria

* Silent cerebral infarction * Cerebral infarction due to other causes except artery scleroses (i.e. cardiogenic embolism, hypercoagulable state, endangium stripping, vasculitis) * Presence of serious heart disease, heart, liver, lung, and kidney functional failure; malignancy; alimentary tract hemorrhage mental disorder and noncooperation with physician * Females during pregnancy or lactation * Already attend other clinical trial

Design outcomes

Primary

MeasureTime frame
recurrence of stroke1 year

Secondary

MeasureTime frame
incidence rate of cardiovascular events, and peripheral arterial events1 year

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026