The Diagnostic Value of Acupoint Sensitization Based on Stable Angina Pectoris
NCT ID: NCT03341663
Last Updated: 2024-05-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
183 participants
OBSERVATIONAL
2017-12-06
2018-11-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Interventions
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Coronary angiography,Canadian Cardiovascular Society angina pectoris classification for the severity of angina and electronic Von Frey instrument for testing the degree of acupoint sensitization
All the interventions were tested for only once
Eligibility Criteria
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Inclusion Criteria
* The frequency of angina attacks were greater or equal to twice a week over the previous 3 months
* Patients agree to do coronary angiography examination and sign the informed consent.
Exclusion Criteria
* Patients who can't accomplish the detection of acupoint sensitization
* Patients with allergic condition, especially the contrast media
* Patients with acute myocardial infarction, unstable angina, during arrhythmia and serious diseases which can affect the blood supply of myocardial
* Patients with skin or peripheral nerve paresthesia, pain or the detect area of skin ulcerate
* Pregnant or lactating women
* Patients who undergoing other clinical trials
35 Years
80 Years
ALL
No
Sponsors
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West China Hospital
OTHER
Responsible Party
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Sun Xin
Director
Locations
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The West China Hospital of Sichuan university
Chengdu, Sichuan, China
Countries
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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201781590955
Identifier Type: -
Identifier Source: org_study_id
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