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Study on Database Construction of Fainting

Study on Database Construction of Fainting - ILR study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1050230051
Enrollment
550
Registered
2023-06-25
Start date
2023-06-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

syncope

Interventions

None listed

Sponsors

Kengo Kusano
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients 18 years of age or older who visited our hospital for syncope between April 1, 2022 and December 31, 2025. 2) Patients whose "syncope template" is recorded by the attending physician in the medical record of the National Cerebral and Cardiovascular Center.

Exclusion criteria

Exclusion criteria: If the consent of the individual cannot be obtained or if the individual requests refusal to participate

Design outcomes

Primary

MeasureTime frame
Establishment of a database of syncope patients

Secondary

MeasureTime frame
Diagnostic flowchart of TLOC cases, including the rate of confirmed diagnosis (and the rate of unexplained deaths) Rates of sudden death and the period from the date of initial visit to the sudden death. Rate of repeated syncope after the initial visit (if yes, whether or not there was an injury at the time of syncope) Rates of invasive interventions (e.g., implantable cardiac devices, catheterization, or surgery) Total number of tests performed to reach a definitive diagnosis (including ILR) Percentage of treatment modalities (lifestyle guidance, drug therapy, catheter/device therapy, etc.) for syncope The number of patients with syncope who received treatment for syncope (including ILR). The period from the date of the first visit (defined as the date of the first visit to the clinic as syncope) to the date of definitive diagnosis. The number of tests performed before ILR implantation and the period from the date of the first visit to the date of ILR implantation. The rate of definitive diagnosis by ILR and the time from ILR implantation to definitive diagnosis Differences in positive predictive value and time required for data extraction/analysis among ILR manufacturers.

Contacts

Public ContactImai Yoshiko

National Cerebral and Cardiovascular Center

hayashida.yoshiko@ncvc.go.jp+81-661701070

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026