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Study on evidence-based evaluation and transformation application of Wenyang Huoxue Decoction in the treatment of bradyarrhythmia

Study on evidence-based evaluation and transformation application of Wenyang Huoxue Decoction in the treatment of bradyarrhythmia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001468
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Slow arrhythmia

Interventions

Experimental Group:Yang-warming and blood-activating formula decoction
Control Group:Heart Treasure Pill

Sponsors

China Academy of Traditional Chinese Medicine, Xiyuan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meets diagnostic criteria for sinoatrial node dysfunction or atrioventricular conduction block; 2. Exhibits corresponding clinical symptoms such as dizziness, transient visual obscurations, fatigue, palpitations, or chest oppression, and considers symptom episodes clearly related to bradycardia; 3. Patient refuses pacemaker therapy; 4. Meets diagnostic criteria for yang deficiency and blood stasis syndrome; 5. Age between 18 and 75 years old; 6. Willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Dynamic electrocardiogram indicates the longest RR interval >3 seconds or the lowest heart rate 160 mmHg or diastolic >100 mmHg); 5. Drug-induced transient secondary bradycardia; 6. Bradycardia caused by hypothyroidism; 7. Glaucoma; 8. Pregnant or breastfeeding women; 9. Suffering from anxiety, depression, or other mental disorders; 10. Coagulation dysfunction; 11. Allergy to the investigational drug; 12. Participation in other clinical trials within the past month; 13. Other conditions deemed unsuitable for participation in the study by the investigator.

Design outcomes

Primary

MeasureTime frame
Lowest heart rate;After 8 weeks of treatment, the symptom-specific VAS scores changed compared to baseline by =13 mm.;

Secondary

MeasureTime frame
Heart Rate Variability Index;Health Condition Questionnaire;Cost-Effectiveness Analysis;Infrared Heatmap;Full-cycle dynamic tongue appearance monitoring;

Countries

China

Contacts

Public ContactZhang Wantong

China Academy of Traditional Chinese Medicine, Xiyuan Hospital

wantong_zhang@hotmail.com13311176716

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026