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A Multicenter Randomized Controlled Trial on the transcutaneous electrical acupoint stimulation of Zusanli/Neiguan for the treatment of chronic coronary syndrome

A Multicenter Randomized Controlled Trial on the transcutaneous electrical acupoint stimulation of Zusanli/Neiguan for the treatment of chronic coronary syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080598
Enrollment
Unknown
Registered
2024-02-02
Start date
2024-02-02
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Chronic Coronary Syndrome

Interventions

Treatment group:TEAS Zusanli/Neiguan+Western medicine
Control group:Western medicine

Sponsors

The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Comply with the 2019 ESC Guidelines for the diagnosis and management chronic coronary syndromes; (2) Stable angina pectoris; (3) The classification criteria for angina pectoris are based on the severity classification of angina pectoris by the Canadian Cardiovascular Society, which is divided into levels I, II, and III; (4) Age ranging from 30 to 80 years old, regardless of gender; (5) Sign an informed consent form and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: (1) Poor control of blood pressure and blood sugar; (2) Severe cardiovascular diseases such as severe cardiopulmonary insufficiency, severe arrhythmia, severe arterial stenosis, dissection, etc; (3) Patients with severe cerebrovascular diseases, liver, kidney or blood system diseases, or malignant tumors; (4) Individuals with bleeding tendencies or allergic constitution; (5) Patients with pacemakers installed; (6) Pregnant or lactating women, or those with fertility requirements in the past six months; (7) Those who have merged mental illnesses or are unwilling to cooperate; (8) Individuals who have participated or are currently participating in other clinical trials within the past 3 months.

Design outcomes

Primary

MeasureTime frame
6-MWT;SAQ;

Secondary

MeasureTime frame
VAS;Electrocardiogram;hs-CRP;Frequency of angina attacks;Usage of Nitroglycerin;Heart rate variability;Blood routine;Urinalysis;Liver function;Renal function;PT APTT TT FIB;

Countries

China

Contacts

Public ContactHanxingjun

The Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine

hanxingjun1228@163.com+86 135 8907 6031

Outcome results

None listed

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