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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01845909
Other study ID # SCD-SOS
Secondary ID
Status Active, not recruiting
Phase N/A
First received April 27, 2013
Last updated June 9, 2017
Start date February 2012
Est. completion date December 2017

Study information

Verified date June 2017
Source University of Coimbra
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

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

Study Design


Intervention

Other:
ECG and survey screening


Locations

Country Name City State
Portugal Unidade Móvel - Tenda de Rastreio - SCDSOS Coimbra State...

Sponsors (4)

Lead Sponsor Collaborator
University of Coimbra Administração Regional de Saúde do Centro, Centro Hospitalar e Universitário de Coimbra, Medtronic

Country where clinical trial is conducted

Portugal, 

Outcome

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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