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Finnish Genetic Study for Arrhythmic Events

Finnish Genetic Study for Arrhythmic Events

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02075866
Acronym
FinGesture
Enrollment
8000
Registered
2014-03-03
Start date
1998-01-31
Completion date
2017-12-31
Last updated
2014-03-04

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

Conditions

Acute Coronary Event, Sudden Cardiac Death

Brief summary

Finnish Genetic Study for Arrhythmic Events (FinGesture is a prospective case-control study assessing the characteristics and genetic background of consecutive series of autopsy verified out-of-hospital victims of SCD vs. survivors of an acute coronary event in a specific geographical area in northern Finland.

Interventions

None listed

Sponsors

University of Oulu
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Sudden cardiac death verified by medicolegal autopsy (cases) * Acute coronary event (increased troponin levels/ECG markers of ischemia/angina pectoris; two out of three criteria) (controls).

Exclusion criteria

* Sudden death due to other causes (cases). * Acute coronary event patients who died during hospitalization (controls).

Design outcomes

Primary

MeasureTime frame
sudden cardiac death20 years

Countries

Finland

Contacts

Primary ContactEeva Hookana, PhD
eeva.hookana@oulu.fi35883154464
Backup ContactJuhani Junttila, MD, PhD
juhani.junttila@oulu.fi358505444367

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026