Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 10:32 PM
Ignite Modification Date: 2025-12-24 @ 10:32 PM
NCT ID: NCT05820035
Eligibility Criteria: Inclusion Criteria: 1. age from 18 to 80 years, 2. episode of PSVT recorded by a 12-lead surface electrocardiogram (ECG), 24-hour Holter monitoring, or esophageal electrophysiologic study (EES) before hospitalization 3. reproducible clinical tachycardia confirmed by the electrophysiological study (EPS). Exclusion Criteria: 1. Previous failure or recurrence of radiofrequency ablation 2. Left ventricular ejection fraction (LVEF) ≤ 40% 3. Combined with atrial flutter or atrial fibrillation 4. Combination of thromboembolic disease 5. Women who are breastfeeding, pregnant or planning to become pregnant during the study period 6. Carrying active implants in the body (e.g., pacemakers, ICDs, etc.) 7. Patients with second-degree (type II) or third-degree atrioventricular block 8. NYHA Class III-IV cardiac function \[Appendix 1\] 9. Patients with congenital heart disease (excluding atrial septal defect and patent foramen ovale) 10. Patients with definite acute cerebrovascular disease (including cerebral hemorrhage, stroke, transient ischemic attack) within the last 1 month 11. cardiovascular events within the last 3 months (including acute myocardial infarction, coronary intervention or heart bypass surgery, prosthetic valve replacement or repair, atrial or ventriculotomy) 12. Acute or severe systemic infection 13. Patients with severe liver and kidney diseases, malignant tumors and end-stage diseases 14. Patients with significant bleeding tendency, hypercoagulable state and serious hematologic disorders 15. Patients who have participated or are participating in other clinical trials within 3 months before enrollment 16. Patients who have other conditions that the investigator considers inappropriate for participation in this trial.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 80 Years
Study: NCT05820035
Study Brief:
Protocol Section: NCT05820035