About this trial
More research is needed to articulate the most effective ways to use these tools as screening tests in cardiovascular risk assessments and how they ultimately affect CVD mortality and morbidity outcomes. Clinicians are encouraged to continue sharing decision-making with patients to combine their unique cardiovascular risk factors and develop a comprehensive, effective treatment plan.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
All individuals attending the preventive cardiology clinics.
Disqualifiers
• Individuals who refused to give consent.
Trial population
Both genders, age 18 and above, visiting preventive cardiology clinics with or without established CVD and may or may not have CVD risk factors.
Trial design
Cohort
Prospective
Treatments tested in this trial
Cardiovascular risk assesment
Other interventionASCVD Score and WHO Cardiovascular Risk score.
Treatment groups
Trial outcomes
Primary outcomes
cardiovascular risk assesesment
risk stratification of Cardiovascular diseases (CVD) in patients without established CVD but with CVD co morbids.we are using Atherosclerotic Cardiovascular Diseases (ASCVD) Risk Score and World Heart Organization(WHO) Risk Score for CVD Risk Assesment. In ASCVD Risk Score, we categorize population into low risk ( score \<5), borderline(score between 5 and 7.4) ,intermediate( score between 7.5 an 19.9) and high risk (score\>20), using all parameters for risk assesment. For WHO risk score calculation we are using WHO Risk score system for South Asia. https://cdn.who.int/media/docs/default-source/cardiovascular-diseases/south-asia.pdf?sfvrsn=c5b0d9a3\_2
Secondary outcomes
Cardiovascular risk reduction
CVD risk reduction in patients with or without established CVD but with CVD co morbids.
Cardiovascular related deaths
Estimation of patients who expired in their follow up despite CVD risk factors management.
Sponsors and contacts
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