DETECTion of the Prevalence of Silent Atherosclerosis Across Adult Life and Development of a Risk Calculator to Predict Its Presence. Phase One of the REACT (Cure of Atherosclerosis) Project

Status: Recruiting
Location: See all (5) locations...
Study Type: Observational
SUMMARY

Atherosclerosis is preventable, yet it continues to significantly contribute to global morbidity and mortality. Atherosclerosis may occur early in life and may present in all vascular territories. The DETECT study's main aim is to determine the prevalence of asymptomatic atherosclerosis (silent) in an adult population of a wide age range of European ancestry through vascular ultrasound (VUS) of peripheral arteries (carotid and femoral territories), as well as establishing the relationship between atherosclerosis in peripheral arteries, coronary arteries, and other vascular territories assessed by computed tomography angiography (CTA). The DETECT study also aims to identify risk factors for development of subclinical atherosclerosis that can hopefully improve the detection of the risk for development of atherosclerotic cardiovascular disease (ASCVD) with far higher precision than currently. In future research, the findings in this descriptive study may eventually be used as part of an age-adapted imaging-based screening for subclinical atherosclerosis. The investigators hypothesize that a precision medicine-based approach to identify candidates likely to benefit from primary prevention against atherosclerosis, may improve medical decision making, by combining traditional risk factors, including lifestyle and psychological factors, phenotypic findings and findings on vascular imaging, and patterns of circulating biomarkers to identify risk of atherosclerosis especially in young individuals and at earlier disease stages (the ultimate population target of REACT project, phase II), maximizing the potential for prevention long before overt disease occurs. An essential aspect of this approach is to pinpoint the specific risk factors in each individual that primarily drive atherosclerosis throughout their life and could serve as therapeutic targets. Thus, the overall purpose of this study is to establish the necessary knowledge, including extensive characterisation of atherosclerosis across life and thus add to the rational foundation for future development of a far more efficient and precise prophylaxis against ASCVD as compared with the presently applied methods.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: t
View:

⁃ The study will include adults ≥18 to ≤70 years of age (1:1 sex ratio in each 10 years age strata).

⁃ Have not been diagnosed with ASCVD prior to inclusion into the study (participants with other cardiovascular diseases or predisposing factors are not excluded).

⁃ The participants will be recruited from sites in Denmark (n \

• 8,000) (and Spain (n \

• 8,000)).

⁃ Participants need to be capable and be able to read and understand Danish, English, Spanish or Arabic.

Locations
Other Locations
Denmark
Rigshospitalet
RECRUITING
Copenhagen
Righospitalet - Glostrup Hospital
RECRUITING
Glostrup Municipality
Herlev Hospital
NOT_YET_RECRUITING
Herlev
Regionshospitalet Gødstrup
RECRUITING
Herning
Spain
Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC)
NOT_YET_RECRUITING
Madrid
Contact Information
Primary
Henning Bundgaard, Professor
henning.bundgaard@regionh.dk
+4535450512
Backup
Anna Ringgaard, PhD
anna.kirstine.ringgaard@regionh.dk
+4535458361
Time Frame
Start Date: 2024-11
Estimated Completion Date: 2032-07
Participants
Target number of participants: 16000
Related Therapeutic Areas
Sponsors
Collaborators: Centro Nacional de Investigaciones Cardiovasculares Carlos III, The Novo Nordic Foundation, Gødstrup Hospital, Herlev and Gentofte Hospital
Leads: Rigshospitalet, Denmark

This content was sourced from clinicaltrials.gov