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Clinical curative effect evaluation research of acupuncture with branch-foundation acupoint combination on prevention and treatment of stable angina

Clinical curative effect evaluation research of acupuncture with branch-foundation acupoint combination on prevention and treatment of stable angina

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012172
Enrollment
Unknown
Registered
2017-07-29
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

stable angina

Interventions

Group 1:embedding-needle with branch-foundation acupoint combination
Group 2:routine selection of acupoints

Sponsors

Hubei Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnosis standard of Western medicine for stable angina pectoris; (2) Aged 35 to 70 years old; (3) The onset time of more than 3 months, and nearly 1 months more than 2 times a week; (4) Within the past week, no other relevant treatment was received; (5) Willing to participate, cooperate with this project research, and adhere to treatment according to plan; (6) Signing the inform consent.

Exclusion criteria

Exclusion criteria: (1) Fail to meet the the diagnosis standard of Western medicine for stable angina pectoris; (2) With acute coronary syndrome, severe arrhythmias, atrial fibrillation, primary cardiomyopathy, valvular heart disease, and acute myocardial infarction in the past three months or more than grade 4 with severe heart disease; (3) The average heart rate < 50 times / min or atrioventricular block; (4) Some special people (who have fertility requirements for the past half year; women who are pregnant or lactating, bleeding, allergic to the constitution, drug addicts, etc.); (5) With hypertension, diabetes treatment failed to meet the standards; (6) Severe neurosis, climacteric syndrome complicated with mental disorders; (7) With cardiovascular disease have been treated with acupuncture in the past 3 month ; (8) Participant in other clinical trials. Meeting any one of the above 8 will not be included in this study.

Design outcomes

Primary

MeasureTime frame
The angina pectoris attack frequency , extent, duration, and the dosage of nitroglycerin before and after treatment;

Secondary

MeasureTime frame
The improvement of ECG and visual analogue scale and VAS score;Angina pectoris scale (SAQ) and SF-36 scale score were used before and after treatment;

Countries

China

Contacts

Public ContactHuang Wei

Hubei Provincal Hospital of Traditional Chinese Medicine

139860883982@qq.com+86 139860883982

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026