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Clinical and Experimental Study on the "Dose-Effect-Form" Relationship of Different Formulations of "Sanshen Liansong Decoction" in the Treatment of Benign Arrhythmia.

Clinical and Experimental Study on the "Dose-Effect-Form" Relationship of Different Formulations of "Sanshen Liansong Decoction" in the Treatment of Benign Arrhythmia.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002540
Enrollment
Unknown
Registered
2025-12-24
Start date
2024-03-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Arrhythmia

Interventions

Usual care group:Conventional medical treatment in Western medicine
Decoction Group:Sanshen Liansong Decoction
Granules Group:Sanshen Liansong Granules
Low-dose granules group:0.7 times the dose of Sanshen Liansong granules

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years and = 80 years gender not limited.; 2. Holter monitoring indicating premature beats with the diagnosis of premature beats meeting both Western and traditional Chinese medicine diagnostic criteria; 3. Willingness to undergo 12 weeks of medication treatment including but not limited to standardized drug therapy such as ß-blockers (unless contraindicated or intolerant the optimal treatment dose should be achieved); 4.Voluntary participation with understanding and signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Potentially malignant or malignant arrhythmias such as atrial flutter and fibrillation; 2. Arrhythmias caused by severe valvular disease congenital heart disease pericardial disease and non-cardiac causes or premature beats due to the failure of important organs like the liver and kidneys; 3. Patients with serious primary diseases affecting the liver kidneys and hematological system renal dysfunction liver transaminases or alkaline phosphatase exceeding three times the normal upper limit blood creatinine > 2mg/dl (176.82umol/L) blood potassium > 5.5mmol/L; cancer patients those with severe neuroendocrine diseases and psychiatric patients and patients with clinically assessed expected survival time of less than 1 year due to malignant progressive diseases; 4. Patients with left ventricular outflow tract obstruction myocarditis aortic aneurysm dissecting aneurysm or unrepaired valvular heart disease causing significant hemodynamic changes; patients with cardiogenic shock uncontrollable malignant arrhythmias second-degree type II or higher sinoatrial or atrioventricular block without pacemaker treatment progressively worsening unstable angina or acute myocardial infarction; 5. Patients planning to undergo cardiac ablation surgery in the near future or those who have already received cardiac resynchronization therapy; 6. Individuals with allergies or known allergies to treatment medications; 7. Individuals who have participated in other drug clinical studies within the past month; 8. Pregnant or preparing for pregnancy and breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Minnesota living with heart failure questionnaire;24-hour premature beat count;

Secondary

MeasureTime frame
Improvement of palpitations and chest tightness;TCM Syndrome Points;ECG rhythms;Composite endpoint events;

Countries

China

Contacts

Public ContactDing Banhan

Guangdong Provincial Hospital of Chinese Medicine

13682238225@139.com+86 136 8223 8225

Outcome results

None listed

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