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

Sponsor: University Hospitals, Leicester

NCT ID: NCT04388943

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Observation (other)
How long the study runs
Study runs about 201 months (dates as stated)
About the drug or intervention
Observation — other: Physiological Measurements Patient reported questionnaire Blood sampling
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years to 90 Years
Who
All
Number of participants
9,500
Started
2010-06-17
Last checked
2026-06

Plain English Summary

What is this study?

  • • Testing a new treatment for cardiovascular diseases
  • • Clinical study - 9,500 participants
  • • 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

Who can take part?

  • • Ages 18 Years to 90 Years
  • • Diagnosed with cardiovascular diseases

Where?

  • • Leicester - University Hospitals Leicester

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Cardiovascular DiseasesCardiovascular Risk Factor

How this trial compares with your answers

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 90 Years
  • Who can join: All genders

What the study is looking for

  • ✓All outpatients and inpatients with cardiovascular disease, of either gender
  • ✓Aged 18-90 years old
  • ✓Healthy volunteers
  • ✓From the community without cardiovascular or other diseases

Who cannot take part

  • ✗Any patient who is unable to give consent
  • ✗Any patient with non-cardiovascular other health condition 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
See the full criteria
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

Where Is This Study? (1 UK site)

University Hospitals Leicester

Leicester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Carolyn Maloney

uhl-tr.researchandinnovationadminmailbox@nhs.net0116 258 8351

How to Get in Touch

Emma P Beeston

Sponsor contact

CONTACT

0116 204 4738 emma.beeston@uhl-tr.nhs.uk

Tara Maitland

Sponsor contact

CONTACT

0116 204 4737 tara.maitland@uhl-tr.nhs.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-06