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Registry on Microvascular Dysfunction and Coronary Spasm

Multicenter Registry on Microvascular Dysfunction - Searching a New Ach Spasm Definition

Recruiting Observational Study
Coronary Microvascular Disease Coronary Vasospasm
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 90
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
Johannes Gutenberg University Mainz · Other
Who this trial is looking for

This trial is looking for patients who are being checked for issues with blood flow in the heart's small vessels and coronary spasms. Participants will help researchers gather important information about these conditions in Europe and North America.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have had tests measuring blood flow and pressure in my coronary arteries.

You may not be able to join if

  • I am experiencing hemodynamic instability.
  • I am under 18 years old.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

The MICRO-SNAPE registry will collect data from patients undergoing investigation of microvascular dysfunction and coronary spasm in Europe and North America.

Trial Locations

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Eligibility Criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Hemodynamic instability * Age \<18 years
Contacts

No contact information available.

NCT ID: NCT06125392 Source: ClinicalTrials.gov