Cardiomyopathies Clinical Trial
— SCD-SOSOfficial title:
Sudden Cardiac Death: Evaluation of a New Strategy to Identify Young Adults at Risk
Verified date | June 2017 |
Source | University of Coimbra |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The investigators have created a way of quickly collecting information in a large scale
young population regarding the presence of some severity indicators that may allow us to
classify them into: seemingly "low risk" and possible "elevated risk" for the presence of
heart disease. It would have to be a short questionnaire, in order to receive a great
adherence but that could simultaneously provide precise information, with an adequate
description of symptoms and warning signs, in a way that a triage in the young adult
population could be performed in the general young adult population in order to select
individuals with an indication for personalized clinical evaluation and possible need of
complementary diagnostic means. Based on this premise the investigators have developed a
fast-response questionnaire named the Sudden Cardiac Death Screening Of risk factorS
(SCD-SOS). This questionnaire has already been tested in a population of approximately 1500
young adults, and some changes have been introduced in order to refine its performance.
To best of the investigators knowledge, there are no large scale European surveys estimating
the prevalence of cardiac disease and associated clinical symptoms in a non-selected
(non-athlete) population of this age group.
Purpose: To screen a young adult population from central regional of Portugal for heart
disease possibly associated to a high risk of Sudden Cardiac Death (SCD).
To determine the national prevalence of clinical symptoms of heart disease and of heart
disease with increased risk for SCD in this age group.
To detect young adults in risk of SCD and with an indication for evaluation by a
cardiologist, and possible need of:
- medical treatment
- electrophysiologic (EP) study and percutaneous ablation
- an implantable cardiovertor defibrillator
- a pacemaker
- other type of specialized cardiac intervention
Status | Active, not recruiting |
Enrollment | 15351 |
Est. completion date | December 2017 |
Est. primary completion date | May 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 12 Years to 40 Years |
Eligibility |
Inclusion Criteria: - 12 to 40 years of age - Providing an informed consent Exclusion Criteria: - Failure to meet any of the aforementioned inclusion criteria |
Country | Name | City | State |
---|---|---|---|
Portugal | Unidade Móvel - Tenda de Rastreio - SCDSOS | Coimbra | State... |
Lead Sponsor | Collaborator |
---|---|
University of Coimbra | Administração Regional de Saúde do Centro, Centro Hospitalar e Universitário de Coimbra, Medtronic |
Portugal,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Type 1 electrocardiogram | Presence of ECG changes suggestive of cardiac disease associated with an increased risk of sudden cardiac death. Definition present in: Corrado D et al. Recommendations for interpretation of 12-lead electrocardiogram in the athlete. Eur Heart J 2010;31:243-259 |
baseline | |
Primary | Clinical History - Red Flag | Presence of answers concerning symptoms or past family history that are known to be associated with increased risk of sudden cardiac death: e.g. effort syncope, syncope with fast palpitations prodrome, know high-risk cardiac disease, history of sudden cardiac death in first or second degree relative |
Baseline | |
Primary | all-cause mortality | occurrence of death of any cause in the participant | First 20 years after enrollement | |
Primary | Cardiovascular death | Occurrence of death of cardiovascular etiology during follow-up. | First 20 years after enrollement |
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