Observing complications during heart procedures
Prospective Global Registry of Complications of Percutaneous Coronary Interventions
This study looks at patients having heart procedures to see what complications happen and how they are managed to improve safety and care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 4000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Minneapolis Heart Institute Foundation Academic / other |
| Locations | 1 site (Minneapolis, Minnesota) |
| Trial ID | NCT05100940 on ClinicalTrials.gov |
What this trial studies
This observational registry focuses on patients undergoing coronary angiography and percutaneous coronary intervention (PCI) to assess the frequency and types of complications that arise during these procedures. It aims to document the procedural strategies used to manage these complications and evaluate the immediate and long-term clinical outcomes for patients affected. By systematically studying these complications, the registry seeks to enhance procedural safety and optimize patient care.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who are undergoing coronary angiography or PCI and experience a complication during or after the procedure.
Not a fit: Patients who do not experience any complications during their cardiac procedures may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved safety protocols and better management strategies for patients undergoing PCI.
How similar studies have performed: Other observational studies have shown success in identifying and managing complications in similar cardiac procedures, indicating that this approach is both relevant and valuable.
Eligibility criteria
Show full inclusion / exclusion criteria
* Over 18 years of age * undergoing coronary angiography or PCI * A complication occurred during or after the procedure
Where this trial is running
Minneapolis, Minnesota
- Minneapolis Heart Institute Foundation — Minneapolis, Minnesota, United States (Recruiting)
Study contacts
- Study coordinator: Emmanouil Brilakis, MD, PhD
- Email: emmanouil.brilakis@allina.com
- Phone: 612-863-3852
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.