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Clinical characteristics and prognosis in syncope patients: A single-center, prospective cohort study

Clinical characteristics and prognosis in syncope patients: A single-center, prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074999
Enrollment
Unknown
Registered
2023-08-22
Start date
2018-06-01
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Syncope

Interventions

Case series:None

Sponsors

The Second Hospital of Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? Age =18 years old; ? Clinical symptoms were consistent with the characteristics of syncope; ? Patients and their family members understood the purpose and procedure of this study, voluntarily participated in this study, and signed written informed consent; ? Patients and their family members were willing and able to adhere to the study plan and other protocol requirements.

Exclusion criteria

Exclusion criteria: ? Inability to sign written informed consent; ? Loss of consciousness due to other causes, such as vertigo, coma, shock, seizures, head injury, transient ischemic attack, drug toxicity, hypoglycemia; ? Pregnant women; ? History of drug or alcohol abuse.

Design outcomes

Primary

MeasureTime frame
Syncope recurrence;All-Cause Mortality;Major adverse cardiovascular events;

Secondary

MeasureTime frame
Quality of life;

Countries

China

Contacts

Public ContactTong Liu

The Second Hospital of Tianjin Medical University

liutongdoc@126.com+86 139 0218 3163

Outcome results

None listed

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