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Cardio-Renal Registry

Barts Health Cardio-Renal Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06521801
Acronym
BHCRR
Enrollment
60000
Registered
2024-07-26
Start date
2024-08-01
Completion date
2030-06-01
Last updated
2026-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardio-Renal Syndrome, Cerebrovascular Accident, Dialysis, End Stage Renal Disease, Myocardial Infarction, Percutaneous Coronary Intervention

Brief summary

Cardiovascular disease is the leading cause of morbidity and mortality among patients with chronic kidney disease (CKD). Even after adjustment for known cardiovascular risk factors, including diabetes and hypertension, mortality risk progressively increases with worsening CKD. As glomerular filtration rate (GFR) declines the probability of developing coronary artery disease (CAD) increases linearly, and patients with GFR \<60 mL/min/1.73 m2 have 2-3-fold increased CV mortality risk, relative to patients without CKD. Management of CAD is complicated in CKD patients due to the likelihood of comorbid conditions and potential for side effects. Despite their high cardiovascular risk, ACS patients with renal dysfunction are less commonly treated with guideline-based medical therapy and are less frequently referred for coronary revascularisation. This observation, referred to as the treatment risk paradox, has been well described and may be explained by physicians' concerns regarding possible nonrenal side effects as well as renal toxicities. Furthermore, patients with severe CKD have traditionally been under-represented in most large cardiovascular clinical trials. Therefore, recommendations for both medical and revascularisation of CAD have relied heavily on extrapolation of results from the non-CKD population. This data will add to that literature by assessing the characteristics and outcomes of patients with CAD and CKD. It will also identify and characterise predictors of outcomes, improve risk stratification and diagnostic evaluation.

Interventions

OTHERObservation

Observation

Sponsors

Queen Mary University of London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Informed consent will not be sought for, as patients are automatically included onto a database that we will use for research purposes. No children will be included in this study. Vulnerable adults or those unable to give consent will be included in the study as well if they are referred to the Nephrology team. Inclusion Criteria: 1. Both male and female patients ≥16 years of age will be included 2. All patients will be reviewed by the Nephrology team a the RLH with renal disease.

Exclusion criteria

1\. Patients \<16 years will not be included in this study.

Design outcomes

Primary

MeasureTime frame
Mortality30 days and 1 year
Re-admission rates30 days and 1 year
Major Adverse Cardiac Events30 days and 1 year
Major Adverse Kidney Events30 days and 1 year

Countries

United Kingdom

Contacts

Primary ContactKrishnaraj Rathod, MBBS, PhD
k.s.rathod@qmul.ac.uk02073777000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026