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Compatibility rule mining of traditional Chinese medicine based on Beiji Qianjin Yaofang and Qianjin Yifang on Palpitation treatment, and its clinical research on intervention of ventricular premature complexes

Compatibility rule mining of traditional Chinese medicine based on Beiji Qianjin Yaofang and Qianjin Yifang on Palpitation treatment, and its clinical research on intervention of ventricular premature complexes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051308
Enrollment
Unknown
Registered
2021-09-18
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

Ventricular Premature Complexes

Interventions

Sponsors

Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of Western medicine for premature ventricular contractions; the frequency of premature ventricular contractions is classified as Myerburg grade 3-4 and the morphology is classified as A-D; patients with premature ventricular contractions with 500 beats/24h<=premature beats<=10000 beats/24h; 2. Patients with premature ventricular contractions of yin and yang deficiency type based on TCM syndrome differentiation; 3. Aged 18-75 years old; 4. Have not participated in other drug clinical trials before being selected; 5. Voluntarily participate in this clinical study and sign the informed consent form, insist on taking the medicine for 4 weeks, and complete the pre-treatment and post-treatment questionnaires, blood tests, and follow-up work with fixed contact information.

Exclusion criteria

Exclusion criteria: 1. Combined with bradyarrhythmia (<50 beats/min) including sick sinus syndrome and atrioventricular block (second or third degree atrioventricular block); 2. Sustained ventricular tachycardia, non-sustained ventricular tachycardia and persistent atrial fibrillation; 3. Serious illness requiring other antiarrhythmic drugs or associated with other serious illnesses; 4. Arrhythmias caused by drugs, electrolyte disturbances, acid-base balance disorders, emotions and other factors; 5. Patients with unstable angina pectoris, myocardial infarction and various cardiomyopathy of coronary heart disease; uncontrolled hypertension, such as grade 3 hypertension or higher risk, or severe hypotension; uncontrolled diabetic patients; liver and kidney In functional tests, alanine aminotransferase or aspartate aminotransferase exceeds 1.5 times the upper limit of the normal reference value, urea nitrogen exceeds 1.2 times the upper limit of the normal reference value, and serum creatinine exceeds the upper limit of the normal reference value; severe respiratory dysfunction or asthma Patients with primary hematopoietic system diseases, other system diseases (such as hyperthyroidism, etc.), poor peripheral circulation perfusion, severe peripheral vascular disease and premature ventricular contractions of unknown etiology; 6. Allergic, mentally ill, heavy drinker, smoker; 7. Pregnant or lactating women; 8. Those who are taking beta-blockers or have contraindications to beta-blockers; 9. Those who have participated in other clinical trials in the past 3 months or those who are considered inappropriate by the investigators.

Design outcomes

Primary

MeasureTime frame
Number of premature ventricular beats;Tpeak-end interval;Tpeak-end dispersion;QT dispersion;

Secondary

MeasureTime frame
Total heart rate;Maximum heart rate;Minimum heart rate;Average heart rate;Blood routine;Hepatic function test;Renal function test;Generalized Anxiety Disorder-7 (GAD-7);Patient Health Questionnaire-9 (PHQ-9);Self-Rating Depression Scale (SDS);Self-Rating Anxiety Scale(SAS);TCM Symptom Scale;

Countries

China

Contacts

Public ContactHe Qingyong

Guang'anmen Hospital China Academy of Chinese Medical Sciences

heqingyongg@163.com+86 13581965248

Outcome results

None listed

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