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The Diagnostic Value of Acupoint Sensitization Based on Stable Angina Pectoris

The Diagnostic Value of Acupoint Sensitization Based on Stable Angina Pectoris

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03341663
Enrollment
183
Registered
2017-11-14
Start date
2017-12-06
Completion date
2018-11-29
Last updated
2024-05-09

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

Conditions

Acupoint Sensitization, Correlation Analysis, Diagnostic Value, Stable Angina Pectoris

Keywords

Stable Angina Pectoris, Acupoint sensitization, Correlation analysis, Diagnostic value

Brief summary

Investigators adopt cross-sectional study design to carry out the exemplary research in the aspects of disease diagnosis.This study is designed to confirm the hypothesis acupoint sensitization is associated with a severity of angina pectoris, which may contribute to the diagnosis of stable angina pectoris. After the eligible participants recruited in group, the coronary artery lesions will be evaluated through coronary angiography and the Canadian Cardiovascular Society(CCS) angina pectoris classification will also be evaluated at the same time. The degree of acupoint sensitization will be tested by the electronic Von Frey instrument by one professional acupuncturist with total 12 acupoints, including Shenmen,Yinxi, Shaohao,Jiquan,Neiguan, Ximen, Quze, Shanzhong, Juque, Jueyinyu, Xinyu, Duyu. Analysis were conducted to explore relationships between the degree of acupoint sensitization, the degree of coronary artery stenosis and CCS angina pectoris classification. Diagnostic value will be further analyzed in the final step.

Interventions

COMBINATION_PRODUCTCoronary 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

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
35 Years to 80 Years

Inclusion criteria

* Patients meet the diagnostic criteria of ACC/AHA angina pectoris of coronary heart disease * 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

* People with mental disabilities and intelligent obstacle * 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

Design outcomes

Primary

MeasureTime frameDescription
The degree of acupoint sensitizationAbout 1 hourThe value will be obtained through the electronic Von Frey instrument
The degree of coronary artery stenosisAbout 2 hoursData will be obtained through coronary angiography
Canadian Cardiovascular Society angina pectoris classificationAbout 1 hours

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026