Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsN/A

Cardio-Renal Registry

Sponsor: Queen Mary University of London

NCT ID: NCT06521801

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 70 months (dates as stated)
About the drug or intervention
Observation — other: Observation
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
16 Years and over
Who
All
Number of participants
60,000
Started
2024-08-01
Last checked
2026-01

Plain English Summary

What is this study?

  • • Testing a new treatment for end stage renal disease
  • • Clinical study - 60,000 participants
  • • Cardiovascular disease is the leading cause of morbidity and mortality among patients with chronic kidney disease (CKD)

Who can take part?

  • • Ages 16 Years and over
  • • Diagnosed with end stage renal disease

Where?

  • • London - Barts Health NHS Trust

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

About This Trial

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.

End Stage Renal DiseaseCardio-Renal SyndromeMyocardial InfarctionCerebrovascular AccidentPercutaneous Coronary InterventionDialysis

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

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: 16 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Both male and female patients ≥16 years of age will be included
  • ✓All patients will be reviewed by the Nephrology team a the RLH with kidney disease.

Who cannot take part

  • ✗1\. Patients \<16 years will not be included in this study.
See the full 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.

Where Is This Study? (1 UK site)

Barts Health NHS Trust

London EC1A 7BE, United Kingdom

Recruiting
Site contact (verified)
Krishnaraj Rathod, MBBS, PhD02073777000k.s.rathod@qmil.ac.uk

How to Get in Touch

Krishnaraj Rathod, MBBS, PhD

Sponsor contact

CONTACT

02073777000 k.s.rathod@qmul.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-01