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Clinical Trials/NCT04388943
NCT04388943RecruitingNot Applicable

Biomedical Research Informatics Centre for Cardiovascular Sciences (The BRICCS Study)

University Hospitals, Leicester1 site in 1 country9,500 target enrollmentStarted: June 17, 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
9,500
Locations
1
Primary Endpoint
To improve understanding of disease mechanisms in cardiovascular disease

Study Overview

Brief Summary

This project will examine the diagnosis and prognosis of patients with cardiovascular disease in hospital in- and outpatients and compare their characteristics with normal controls from the community. The cardiovascular diseases studied include coronary artery disease, heart failure, heart attacks, valve disease, cardiac surgery, dysrhythmias, aneurysms, embolism, strokes, peripheral vascular disease and hypertension. Current methods for diagnosis and predicting outcome in patients are limited and may lack accuracy. This study will collect clinical details, and blood and urine samples from patients for analysis of proteins, chemicals and genetic biomarkers which will enable an examination of the pathological mechanisms involved in cardiovascular disease. The data will also be used to improve diagnosis and also improve prediction of outcome in patients (future clinical events such as death, further hospitalisation with cardiovascular disease and the effects of any therapy given to the patients). In this way, we can develop accurate ways of assessing a patient's condition and how it could be effectively managed. The study will last for 20 years.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • All outpatients and inpatients with cardiovascular disease, of either gender
  • Aged 18-90 years old
  • Examples of conditions include: coronary artery disease, heart failure, heart attacks (myocardial infarction), valve disease, cardiac surgery, dysrhythmias (including atrial fibrillation), aneurysms, embolism, strokes, peripheral vascular disease, hypertension (and its complications, such as left ventricular hypertrophy) or those presenting with chest pain
  • Healthy volunteers
  • Aged 18-90 years old
  • From the community without cardiovascular or other diseases

Exclusion Criteria

  • Any patient who is unable to give consent
  • Any patient with non-cardiovascular comorbidity likely to cause death within 6 months
  • Patients know to be infected with HIV, Hepatitis B or any other agent posing an infection risk from unfixed material

Outcomes

Primary Outcomes

To improve understanding of disease mechanisms in cardiovascular disease

Time Frame: 20 Years

The principal objective is to improve upon our understanding of disease mechanisms in cardiovascular disease, using plasma and urine proteins or chemicals and a patient's genetic makeup, which may impact on the diagnosis and assessment of prognosis of cardiovascular disease.

Secondary Outcomes

  • To improve prediction of responses to different treatments, using blood proteins or chemicals and a patient's genetic makeup(20 Years)

Investigators

Sponsor
University Hospitals, Leicester
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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