Registry of patients undergoing heart revascularization procedures
Barts Revascularisation Registry - To Understand the Characteristics, Time-trends and Outcomes in Patients With Coronary Artery Disease at Barts Heart Centre
This study collects information on patients with coronary artery disease who have heart procedures to see how well they do and what factors affect their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 20000 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | Queen Mary University of London Academic / other |
| Locations | 1 site (London) |
| Trial ID | NCT05255705 on ClinicalTrials.gov |
What this trial studies
This observational study collects data on patients with coronary artery disease (CAD) who undergo percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) at one of the largest cardiac centers in Europe. The aim is to assess patient characteristics, outcomes, and predictors of success in real-world settings, contributing to the understanding of treatment efficacy and safety. The study utilizes a password-protected clinical database that includes demographic, clinical, and outcome data from a large cohort of patients over several years.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 16 and older who have undergone angiography and revascularization procedures at the participating center.
Not a fit: Patients under 16 years of age or those who have not undergone revascularization procedures will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of treatment outcomes for patients with CAD, leading to improved risk stratification and personalized care.
How similar studies have performed: Other studies have successfully utilized observational data to improve treatment strategies for CAD, indicating that this approach is both valuable and established.
Eligibility criteria
Show full inclusion / exclusion criteria
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 Interventional Cardiology team. * Both male and female patients ≥16 years of age will be included * All patients will have had an angiogram at BHC. * Any patient who has undergone revascularisation. Exclusion Criteria: • Patients \<16 years will not be included in this study.
Where this trial is running
London
- Barts Health NHS Trust — London, United Kingdom (Recruiting)
Study contacts
- Study coordinator: Dr. Krishnaraj Rathod
- Email: krishnaraj.rathod1@nhs.net
- Phone: 02073773000
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.