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The efficacy and safety of invigorating qi and nourishing Yin for palpitation on recurrence in patients with atrial fibrillation after radiofrequency ablation

The efficacy and safety of invigorating qi and nourishing Yin for palpitation on recurrence in patients with atrial fibrillation after radiofrequency ablation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000636
Enrollment
Unknown
Registered
2024-11-01
Start date
2024-11-15
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

atrial fibrillation

Interventions

Control Group:conventional treatment: Oral amiodarone, rivaroxaban, or dabigatran for 3 months, proton pump inhibitors for 1 month
Treatment Group:On the basis of conventional treatment in Western medicine add Yiqi Yangyin Ding Ji traditional Chinese medicine Qiposhengmai granules

Sponsors

Dongzhimen Hospital Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for atrial fibrillation. (2) Patients undergoing their first radiofrequency ablation procedure. (3) Meet the diagnostic criteria for the Traditional Chinese Medicine syndrome of palpitations and deficient Yin and Qi. (4) Aged between 18-75. (5) Subjects must be informed and willing to sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Confirmed patients with class IV angina pectoris acute myocardial infarction class IV heart failure valve heart disease cor pulmonale hypertrophic cardiomyopathy with atrial fibrillation. (2) Confirmed patients with hyperthyroidism-related atrial fibrillation or dilated cardiomyopathy with atrial fibrillation or patients with thyroid dysfunction. (3) Patients with hypotension or poorly controlled blood pressure (=160/110mmHg) or significant hemodynamic disorders. (4) Patients with severe cardiopulmonary dysfunction accompanied by severe arrhythmias (paroxysmal ventricular tachycardia supraventricular tachycardia etc.). (5) Patients with atrial fibrillation after heart valve replacement or repair surgery. (6) Patients with abnormal liver function kidney function hematopoietic system abnormalities or severe primary diseases such as mental illness. (7) Patients participating in other clinical trials. (8) Presence of any clinically significant abnormalities found during laboratory tests physical examinations and electrocardiogram examinations that may interfere with this trial's research and observation. (9) Pregnant or planning to become pregnant unable to take effective contraceptive measures or lactating women. (10) Patients contraindicated for amiodarone (severe sinoatrial node dysfunction atrioventricular block bradycardia prolonged intervals). (11) Patients allergic to any medication used in this trial. (12) Unwilling to participate in the trial or estimated poor compliance.

Design outcomes

Primary

MeasureTime frame
1-year recurrence rate of AF;

Secondary

MeasureTime frame
life quality score;Evaluation of curative effect of TCM syndrome;Indicators of inflammation;Incidence of cardioversion;Echocardiography indicators;

Countries

China

Contacts

Public ContactQiulei Jia

Dongzhimen Hospital Beijing University of Chinese Medicine

lotusrosa@163.com13161063880

Outcome results

None listed

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