Angina, Stable
Conditions
Keywords
acupuncture, Angina, Stable Angina Pectoris
Brief summary
This trail aims to evaluate the efficacy of acupoints on the specific meridian for chronic stable angina pectoris, compared with acupoints on the other meridian, sham acupoints and waiting-list. And to confirm the specificity of acupoints on meridian.
Detailed description
The basis of acupuncture is the theory of meridians and acupoints. Meridian and collaterals internally pertain to viscera, and externally spread over the extremities. An acupoint is the place where the visceral qi and meridian qi distributed in. besides acupoints are the stimulus points and reactive points for acupuncture to treat the diseases. Selecting the acupoints on the specific meridian is the basic principle of acupuncture. Recently, as to the existence of specificity of acupoints on the meridian has been questioned by many researchers. This trial using chronic stable angina pectoris as a carrier, select the acupoints on the hand shao yin heart meridian and hand jue yin pericardium meridian to treat chronic stable angina pectoris. Compared with acupoints on the other meridian and non-acupoints ,aiming to evaluate the efficacy, furthermore ,to confirm the existence of the specificity of acupoints on meridian.
Interventions
OTHERacupuncture
In each session, we treat bilaterally, 3 times a week and 2 days off a week, each patient in the acupuncture treatment groups will receive 12 sessions of acupuncture treatment over 4 weeks. The whole study period is 20 weeks including 4-week baseline period,4-week treatment period, and 12-week follow-up period. we will investigate at 0 day,4week,8week,12week,16week after randomization。
DRUGBasic treatment
Each group in the basic treatment，Foundation treatment including health education and basic drug therapy. We recommend lifestyle modification for all patients. Modifications include increasing exercise; limiting alcohol consumption; and weight loss; quit smorking etc. Basic medication： Aspirin: 100mg qd; Metoprolol：25mg bid; Ramipril:5mg qd; Atorvastatin:20mg qn.
Sponsors
Hunan University of Traditional Chinese Medicine
Chengdu University of Traditional Chinese Medicine
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
35 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
1.Meet the diagnostic criteria of ACC/AHA angina pectoris of coronary heart disease. 2.35 ≤ age ≤ 80 years of age, both male and female. 3.The onset of angina pectoris≥3 months, and the frequency of angina attack≥2 a week. 4.Patients signed the informed consent.
Exclusion criteria
1. age≤35 or age≥80 2. Pregnant women or women in lactation or women of child bearing potential plan to conceive in the recent six months. 3. Combined with cardiovascular, digestive, respiratory, urinary, blood, nervous, endocrine system, severe primary disease clinical failed to effectively control the disease. 4. Complicated with mental disorders. 5. allergic constitution or bleeding disorder. 6. Patients accompany with acute coronary syndrome (including acute myocardial infarction, unstable angina), severe arrhythmias ( severe atrioventricular block, ventricular tachycardia, heartbeat influence the flow dynamics in supraventricular tachycardia, heartbeat frequent premature beats especially premature ventricular contractions ), atrial fibrillation, primary cardiomyopathy, valvular heart disease. 7. The blood pressure and blood glucose fail to meet the treatment targets. 8. Cardiovascular disease who had been treated with acupuncture during the previous three months. 9. Currently participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of angina attacks | 16 weeks after inclusion | The frequency of angina attack during 4-week. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The dosage of nitroglycerin | 0 day,4, 8, 12, 16 weeks after inclusion | — |
| Six minute walk test | 0 day and 4 weeks after inclusion | Six minute walk test in the evaluation of exercise tolerance |
| Dynamic ECG Observation of the changes of ST-T | 0 day and 4 weeks after inclusion | Dynamic electrocardiogram in six minute walk test to do |
| The severity of angina ( VAS score) | 0 day,4, 8, 12, 16 weeks after inclusion | The VAS score evaluation angina pain severity |
| self-rating anxiety scale | 0 day,4, 8, 16 weeks after inclusion | — |
| The incidence of cardiovascular episode during the 4 months | 4, 8, 12, 16 weeks after inclusion | The incidence of cardiovascular episode during the 4 months(develop into unstable angina, acute myocardial infarction, death) |
| Self-rating Depression Scale | 0 day,4, 8, 16 weeks after inclusion | — |
| The Seattle Angina Questionnaire ( SAQ ) score | 0 day,4, 8, 12, 16 weeks after inclusion | — |
Countries
China
Outcome results
None listed