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Acupuncture for chronic stable angina pectoris at acupoints on the involved meridian: a multi-center, randomized, controlled trial

Not Applicable
Not yet recruiting
Conditions
chronic stable angina pectoris
Registration Number
ITMCTR1900002585
Lead Sponsor
Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. Matching the diagnostic criteria of CSAP according to the Chinese Society of Cardiology;
2. Meeting Class I or II of the Canadian Cardiovascular Society (CCS) angina pectoris severity grade;
3. Aging from 45 to 70 years;
4. Having experienced angina attack in at least the last three months, and the attack frequency >= twice a week in the most recent month;
5. At least 2 months of standardized medication history before enrolment (sustaining the same medication, usage, and dose). Basic therapeutic drug is one or more of the following: ß-blockers, angiotensin converting enzyme inhibitors (ACEIs), angiotensin II receptor blockers(ARB), antiplatelet medications and statins;
6. Having signed informed consent.

Exclusion Criteria

1. Being pregnant or during lactation or intending to be pregnant in the 6 months;
2. Having severe cardiovascular, digestive, urinary, respiratory, hematological, nervous, or endocrine system diseases that cannot be controlled with clinical treat-ments;
3. Converting to acute coronary syndrome (including acute myocardial infarction and unstable angina pectoris), serious arrhythmia (advanced atrioventricular block, ventricular tachycardia, supraventricular tachycardia, frequent premature beats);
4. Being accompanied with serious psychiatric illness;
5. Failing to control hypertension (systolic blood pressure >= 140 mm Hg and/or diastolic blood pressure >= 90 mm Hg) or diabetes mellitus (HbA1 above 7% in last three months);
6. Having received acupuncture therapy due to cardiovascular illness in the last 1 month;
7. Having bleeding tendency and dermatitis;
8. Being in allergic constitution and be allergic to adhesive tape;
9. Participating in any other clinical trials.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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