Actively Recruiting
A Multicenter Registry on the Diagnosis of Patients with Chronic Angina and No Angiographic Coronary Artery Stenosis - Searching a New Acetylcholine Spasm Definition
Led by Johannes Gutenberg University Mainz · Updated on 2024-11-01
1000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting data from patients being tested for microvascular dysfunction and coronary artery spasm in Europe and North America. This observational registry aims to better understand and describe the characteristics of patients with microvascular dysfunction, a condition that significantly affects quality of life but is not well classified. The study focuses on patients with chronic angina without visible coronary artery narrowing. Participants will undergo invasive assessments using coronary pressure wires to evaluate coronary microvascular function and spasm. Measurements include coronary pressure and flow responses to various agents such as acetylcholine, adenosine, and papaverine. Data collected during routine clinical practice will be entered anonymously into the registry. During the study, researchers will analyze invasive measurements to identify different coronary vasomotor function types, assess diagnostic criteria accuracy, and study factors like sex impact and normal coronary flow values. The primary outcome is identification of coronary vasomotor endotypes immediately after invasive testing. Participation involves no additional interventions beyond standard clinical assessments, and data collection is retrospective and observational.
CONDITIONS
Brief Title
Multicenter Registry on Microvascular Dysfunction - Searching a New Ach Spasm Definition
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who underwent combined measurements of coronary pressure and flow in at least 1 native coronary artery in response to endothelium dependent and independent vasodilators.
- Age between 18 and 90 years
You will not qualify if you...
- Hemodynamic instability
- Age under 18 years
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single day procedure
Participants undergo invasive assessment of coronary microvascular dysfunction and coronary spasm using coronary pressure wires and measurements of coronary pressure and flow in response to vasodilators.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Center of Cardiology, Cardiology I, university hospital Mainz
Mainz, Rhineland-Palatinate, Germany, 55131
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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