Vericiguat in Patients With Coronary Microvascular Dysfunction Causing Stable Chest Pain (V-COM)

ConditionChest Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-75
SponsorThe University of Hong Kong

About this trial

This is a randomised controlled trial to determine the effectiveness of Vericiguat to improve stress myocardial blood flow (MBF) and myocardial perfusion reserve as measured by cardiac magnetic resonance (CMR) imaging.

Eligibility criteria

Qualifiers

Stable recurrent chest pain.

40 to 75 years old.

Have coronary computed tomography (CT) angiogram or catheter coronary angiogram within 6 months showing non-obstructive coronary artery disease (<50% coronary artery stenosis or fractional flow reserve >0.8).

Stress CMR MPR <2.19 12 or Stress MBF <2.19ml/g/min 13.

Disqualifiers

Systolic blood pressure <100 mm Hg.

Concurrent use of soluble guanylate cyclase stimulators (eg. Riociguat), or phosphodiesterase type 5 inhibitors (eg. vardenafil, tadalafil, and sildenafil).

Has known allergy or sensitivity to any soluble guanylate cyclase stimulator.

On long-acting nitrates (eg. isosorbide mononitrate)

Trial design

Treatments tested in this trial

  • Vericiguat
  • Stress Cardiac Magnetic Resonance

Treatment groups

94 Participants
are divided into 2 treatment groups

Sponsors and collaborators