Registry for patients with coronary artery disease and microvascular dysfunction
Official title: Mainzer IntraCoronAry daTabase (MICAT). Das Coronary Slow Flow- Syndrom Und Koronare Mikrozirkulationsstörungen- Register.
Run by Johannes Gutenberg University Mainz · NCT02180178 · Data updated 2026-11-12
This study is gathering information from patients with coronary artery disease and microvascular dysfunction to better understand their conditions and improve their care.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Johannes Gutenberg University Mainz Academic / other |
| Locations | 1 site (Mainz) |
| Status | Recruiting |
| Started | September 2013 |
| Main results expected | September 2028 |
| Study ends | September 2028 |
| Registry record updated | October 8, 2024 |
| Trial ID | NCT02180178 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients who have a clinical indication for coronary angiography.
✕Probably not a fit
Patients who do not require coronary angiography or have no related clinical indications may not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry aims to collect prospective data on patients undergoing coronary angiography in Mainz, focusing on those with coronary artery disease and microvascular dysfunction. Patients will be followed up through telephone contacts at various intervals post-procedure, and blood samples will be collected if coronary slow flow is observed. Additionally, the registry will include anonymous retrospective data from patients who underwent routine clinical practice procedures. The goal is to enhance understanding of these conditions and improve patient outcomes.
Why it matters
Potential benefit: If successful, this registry could lead to improved diagnosis and treatment strategies for patients with coronary artery disease and microvascular dysfunction.
How similar studies have gone: Other studies focusing on coronary artery disease and microvascular dysfunction have shown promise, indicating that this approach could yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * clinical indication to coronary angiography Exclusion Criteria: * none
Where it's running
-
University Medical Center Mainz - 2 Medizinische Klinik
Mainz, Germany Recruiting
Study contacts
- Principal investigator: Tommaso Gori, PhD Dott Med e Chirurgia — University Medical Center Mainz
- Study coordinator: Tommaso Gori, PhD, Dott medicina e Chirurgia
- Email: tommaso.gori@unimedizin-mainz.de
- Phone: +49 6131 172829
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
μFR-guided Drug-Coated Balloon Angioplasty vs Angiography-guided Angioplasty in Coronary Artery Disease
This trial tests whether using computational μFR guidance during drug-coated balloon angioplasty is better than standard angiography guidance for people with de novo coronary artery lesions.
-
Gastric Ultrasound Before CABG to See if Heart Function Changes Stomach Contents
This study checks whether people with weaker heart function before elective CABG have different stomach contents seen on ultrasound.
-
Can preoperative photon-counting CT help predict heart recovery after bypass surgery?
This observational study tests whether a preoperative photon-counting CT can help predict heart function 3 months after coronary bypass surgery in adults with coronary artery disease.
-
Real-World Drug-Coated Balloon Angioplasty in Coronary Artery Disease
This registry tests how drug-coated balloons perform in everyday clinical practice for adults with coronary artery disease undergoing PCI.
-
Predicting vasopressor needs after anesthesia in elective on-pump CABG using dynamic arterial elastance
This study tests whether EaDyn measured after induction can help predict which patients will need vasopressors during elective on-pump CABG.
-
Intraoperative Pulse Pressure Variation and Postoperative Lactate Clearance in CABG Patients
This study tests whether the amount a patient’s pulse pressure varies during surgery relates to how quickly lactate levels drop after CABG.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.