- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01825759
Danshen Dropping Pill for Coronary Heart Disease Heart and Artery Structure and Function
April 5, 2013 updated by: Xiaoping Chen, West China Hospital
The Impact of Compound Danshen Dropping Pill for Coronary Heart Disease With Hypertension Patient Heart and Artery Structure and Function
The Impact of Compound danshen dropping pill for coronary heart disease (CHD) heart and artery structure and function in patients with hypertension
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Compound danshen dropping pill for coronary heart disease (CHD) heart and artery structure and function in patients with hypertension.We can accorand the pwv ,IMT and MDA to assess the impact of heart and artery structure and function.
Study Type
Interventional
Enrollment (Anticipated)
200
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: chen xi ping, master
- Phone Number: 028-85423352
- Email: panpei74@163.com
Study Locations
-
-
Sichuan
-
Chengdu, Sichuan, China
- Recruiting
- West China Hospital
-
Contact:
- chen xi ping, master
- Phone Number: 028-85423352
- Email: panpei74@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
35 years to 75 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:coronary heart disease,primary hypertension, -
Exclusion Criteria:secondary hypertension,diabetes mellitus,chronic renal disease,cardiac insufficiency
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: danshen dripping pill
danshen dripping pill 27mg ten pills by mouth every 8 hours for one year
|
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Pulse wave velocity
Time Frame: one year
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
ankle-brachial index
Time Frame: one year
|
one year
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
intima-media thickness,methyl-di-aide-hyde
Time Frame: one year
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: chen xi ping, master, organizer
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2013
Primary Completion (ANTICIPATED)
December 1, 2014
Study Completion (ANTICIPATED)
December 1, 2014
Study Registration Dates
First Submitted
March 26, 2013
First Submitted That Met QC Criteria
April 5, 2013
First Posted (ESTIMATE)
April 8, 2013
Study Record Updates
Last Update Posted (ESTIMATE)
April 8, 2013
Last Update Submitted That Met QC Criteria
April 5, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- West China Hospital
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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