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Impact of Biomarkers on the Response to Cardioneuroablation in Vasovagal Syncope Patients (BRAVE): A National, Multi-center, Prospective, Observational Case-Control Study

Impact of Biomarkers on the Response to Cardioneuroablation in Vasovagal Syncope Patients (BRAVE): A National, Multi-center, Prospective, Observational Case-Control Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101625
Enrollment
Unknown
Registered
2025-04-27
Start date
2025-06-01
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Vasovagal syncope

Interventions

Non recurrent group:NA
Recurrent group:NA

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age is 18~65 years old; 2. Meets the diagnostic criteria for VVS in the 2018 European Society of Cardiology Guidelines for the Diagnosis and Management of Syncope and is determined to be treated with CNA as clinically warranted; 3. The number of syncope episodes >= 3 times, and at least 1 episode of syncope within half a year; 4. Voluntary participation in the study, signed informed consent;

Exclusion criteria

Exclusion criteria: 1. Presence of other possible causes of syncope, such as organic heart disease, arrhythmias, or vertebrobasilar artery abnormalities; 2. History of pacemaker, ICD, or CRT-D implantation; 3. Cardiovascular disease: myocardial infarction within 6 weeks, severe cardiac insufficiency (New York Heart Association cardiac function class III.~IV.); 4. Neurological disorders: history of stroke or transient ischemic attack, epilepsy; 5. Diseases of the endocrine system: diabetes, thyroid diseases; 6. Infectious diseases: hepatitis B, hepatitis C, syphilis, etc. 7. Have a severe mental illness or cognitive dysfunction, unable to understand the content of the study or follow the requirements of the study; 8. Pregnant, lactating women or planning to become pregnant during the follow-up period; 9. Participated in other clinical trials in the past three months; 10. Refused to sign the informed consent form to participate in this study;

Design outcomes

Primary

MeasureTime frame
Time to the first syncope recurrence;Levels of biomarkers;

Secondary

MeasureTime frame
Heart rate and rhythm;

Countries

China

Contacts

Public ContactLi Guoliang

The First Affiliated Hospital of Xi'an Jiaotong University

liguoliang_med@163.com+86 29 85323524

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026