Actively Recruiting

Age: 18Years - 90Years
All Genders
ID06125392

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

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Hemodynamic instability
  • Age under 18 years

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

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

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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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