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Clinical study onTranscutaneous electrical acupoint stimulation of Zusanli/Neiguan combined with conventional Western medicine treatment for myocardial reperfusion injury after cardiac stent surgery

Clinical study onTranscutaneous electrical acupoint stimulation of Zusanli/Neiguan combined with conventional Western medicine treatment for myocardial reperfusion injury after cardiac stent surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082515
Enrollment
Unknown
Registered
2024-03-31
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

Myocardial Infarction Reperfusion Injury

Interventions

Treatment group:Conventional clinical western medicine treatment + transcutaneous acupoint electrical stimulation of the ST36(Zu SanLi)/PC6 ( Nei Guan ) treatment, using transcutaneous electrical stim
Control group:Conventional clinical western medicine treatment + transcutaneous acupoint electrical stimulation of the ST36(Zu SanLi)/PC6 ( Nei Guan ) treatment, using transcutaneous electrical stimul

Sponsors

The Third Affiliated Clinical Hospital of Changchun University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for acute ST-segment elevation myocardial infarction in the 2017 edition of the European Society of Cardiology Guidelines; 2. Patients receiving emergency PCI treatment for the first time with acute chest pain symptoms<12 hours; 3. Gender unlimited, age = 18 years old,<80 years old, subject to informed consent; 4. Abnormal elevation of myocardial injury markers;

Exclusion criteria

Exclusion criteria: 1.Previous history of myocardial infarction, coronary stent implantation, or coronary artery bypass grafting; 2. patients with severe heart failure, ECG showing right and left ventricular hypertrophy, intraventricular differential conduction, pre-excitation syndrome, and extreme cis-clockwise transposition, ventricular fibrillation, and post-cardiopulmonary resuscitation; 3. Killip cardiac function = grade 4; 4. patients with malignant tumors, severe infectious diseases, inflammatory diseases, autoimmune diseases, hematologic diseases, and acute cerebral infarction; 5. Participation in any other drug study or therapeutic study using an unapproved drug within the previous 3 months. Note: Patients who meet any 1 of the above criteria are excluded.

Design outcomes

Primary

MeasureTime frame
Infarct Size;

Secondary

MeasureTime frame
Left ventricular ejection fraction;NT-proBNP;IL-6;IL-1ß;TNF-a;Major adverse cardiovascular events;CK-MB;MYO;

Countries

China

Contacts

Public ContactHongfeng Wang

The Third Affiliated Clinical Hospital of Changchun University of Traditional Chinese Medicine

ccwhf@126.com+86 139 4319 3886

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 25, 2026