Coronary Microvascular Disease

14

Review clinical trials related to Coronary Microvascular Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Self-Expanding Coronary Sinus Reducer for Treatment of Symptomatic Coronary Microvascular Dysfunction (CMD) (SERRA-I Study)

VahatiCor's Coronary Sinus Reducer (A-FLUX) has been designed to improve angina or angina-like symptoms in patients with CMD. SERRA-I is an early feasibility study that evaluates the safety and clinical performance of the A-FLUX Reducer in this population.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: VahatiCor, Inc.Updated: May 15, 2026Locations: 3
Eligibility criteria

Older than 18 years of age. [+8]

Significant obstructive epicardial disease (greater than 50% diameter stenosis)... [+18]

Status: Recruiting

Coronary Flow During Rapid Heart Rates

The goal of this observational study is to learn about the factors which determine how well ventricular tachycardia (VT) is tolerated. The main questions it aims to answer are: 1. What impact does coronary artery disease have on the ability for a patient to tolerate VT? 2. Does treatment of coronary artery disease with stents improve the tolerability of VT? Participants who are undergoing a clinically indicated coronary angiogram or coronary angioplasty procedure will have measurements of blood pressure, coronary pressure and coronary flow made during pacing at a range of heart rates.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Imperial College LondonUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Able to give valid consent [+2]

Unable to give valid consent [+5]

Status: Recruiting

Barts-MINOCA Registry

The last 15 years the introduction of primary angioplasty has radically improved outcomes for acute myocardial infarction (AMI). However, the system wide availability of prompt investigation has revealed an important group of patients where progress has stalled, the diagnosis is unclear and therapeutic approaches are uncertain. Myocardial infarction with non-obstructive coronary arteries (MINOCA) is found in 1 - 13% of all patients with a clinical diagnosis of AMI. These patients present a therapeutic predicament since coronary revascularization is not appropriate. Guidelines do not exist for their management - yet the condition is not benign - the 12-month prognosis, although better than obstructive coronary artery disease patients is still guarded with recent data suggesting many questions remain unanswered.

Participants needed: 3,000
Trial details
Age: 16+Biological sex: AllType: ObservationalSponsor: Queen Mary University of LondonUpdated: Nov 18, 2025Locations: 1Duration: 5 Years
Eligibility criteria

Both male and female patients ≥16 years of age will be included [+1]

Patients <16 years will not be included in this study.

Status: Recruiting

Study Targeting Myocardial Perfusion and Symptom Relief in Women With SGLT2 Inhibitors (STRONG)

The goal of this clinical trial is to that Sodium-glucose cotransporter 2 inhibitors treatment will improve Coronary Microvascular Disease with anginal symptoms associated with non-obstructive coronary disease in women. The main questions it aims to answer are: Aim 1: Test the hypothesis that Sodium-glucose cotransporter 2 inhibitors treatment improves coronary microvascular disease in women with no evidence of epicardial obstructive coronary artery disease. Aim 2: Test the hypothesis that Sodium-glucose cotransporter 2 inhibitors treatment improves angina symptoms and other quality of life measurements associated with the improvement of CFR. AIM 3: Identify the effect of Sodium-glucose cotransporter 2 inhibition on inflammation pathways and markers of systemic Research will compare Brezavvy to placebo Participants will: * Take study drug or placebo for 12 weeks * Stress Cardiac magnetic resonance imaging * 12 lead electrocardiograms * Complete questionnaires

Participants needed: 150
Trial details
Phase: Phase 1Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Oct 29, 2025Locations: 1
Eligibility criteria

• Female sex. [+6]

History of non-ischemic cardiomyopathy LVEF <40% or hypertrophic cardiomyopathy. [+19]

Status: Not yet recruiting

A Study of Microcirculatory Function in Type 2 Myocardial Infarction (T2MI)

The purpose of this research is to find out if patients with Type 2 Myocardial Infarction (T2MI) without significant epicardial coronary artery disease (CAD) have a greater chance of having coronary microvascular disease (CMD).

Participants needed: 52
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Mayo ClinicUpdated: Aug 28, 2025Locations: 1
Eligibility criteria

Ability to give informed consent [+3]

Acute coronary event (evidence of plaque rupture, fissure or dissection on coron... [+6]

Status: Recruiting

An Observational Study of Coronary Microvascular Disease of China

Non-obstructive coronary heart disease refers to patients with angina pectoris without significant narrowing of the epicardial vessels. Coronary microvascular disease(CMD) is a kind of non-obstructive coronary heart disease, and its clinical detection rate is increasing, seriously affecting the quality of life of patients, and increasing the risk of cardiovascular adverse events, but its mechanism has not been fully understood. This study will prospectively collect patients who meet the diagnosis of CMD, observe the development and outcome of the disease, and explore its occurrence and development mechanism.

Participants needed: 500
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Henan Institute of Cardiovascular EpidemiologyUpdated: Aug 20, 2025Locations: 1Duration: 3 Years
Eligibility criteria

Angina symptoms [+2]

People under the age of 18 [+1]

Status: Recruiting

A Clinical Study of Fundus OCTA for the Identification of CMD

Coronary microvascular dysfunction (CMD) carries an increased risk of adverse cardiovascular clinical outcomes. The association between fundus microcirculation changes and coronary microcirculation is not well understood. Optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) is a new type of optical diagnostic imaging technology for non-invasive detection, which can perform multi-dimensional quantitative assessment of fundus microcirculation. In this study, investigators intend to use the coronary angiography-derived index of microvascular resistance (caIMR) to screen patients with CMD, explore the relationship between relevant parameters based on OCT and OCTA measurements and caIMR, and evaluate the feasibility and clinical value of non-invasive identification of CMD through fundus OCT and OCTA.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Peking University First HospitalUpdated: Aug 12, 2025Locations: 1
Eligibility criteria

Patients who underwent coronary angiography in the Department of Cardiology, Pek... [+4]

Present serious fundus disease [+6]

Status: Not yet recruiting

Clinical Evaluation of Aromatic Wentong in the Treatment of Coronary Microvascular Disease

Coronary Microvascular Disease (CMD) is a condition where patients experience chest pain (angina) even though their coronary arteries appear normal on angiography. It is common among people with coronary heart disease, especially those with chest pain as their main symptom. Unfortunately, there are no effective treatments available for these patients, and symptoms like chest tightness and persistent pain greatly affect their quality of life. Traditional Chinese Medicine (TCM) suggests that the root cause of microvascular disease is blocked collateral blood vessels. Aromatic Wentong, a TCM approach, aims to improve blood flow and relieve blockages. Kuangxiong Aerosol is a Chinese patent medicine developed based on the principles of Aromatic Wentong. This study is a multicenter, randomized, double-blind, placebo-controlled trial involving 528 patients with chest pain and suspected CMD. Participants are recruited from several hospitals, including China-Japan Friendship Hospital, Fuwai Hospital, and Xiyuan Hospital. Patients are randomly divided into two groups: The intervention group receives standard guideline-recommended treatment plus Kuangxiong Aerosol. The control group receives standard treatment plus a placebo version of Kuangxiong Aerosol. The treatment lasts for 8 weeks.

Participants needed: 528
Trial details
Phase: Phase 4Age: 18-80Biological sex: AllType: InterventionalSponsor: China-Japan Friendship HospitalUpdated: Apr 11, 2025Locations: 1
Eligibility criteria

Aged between 18 and 80 years, regardless of gender. [+7]

Significant liver or kidney dysfunction, defined as ALT, AST, or blood creatinin... [+5]

Status: Recruiting

Impact of Exercise Training on Ischemia With Non-Obstructive Coronary Arteries (INOCA): The ExINOCA Study

The purpose of the study is to identify causes of chest pain in patients experiencing chest pain with no signs of narrowing of the coronary arteries of the heart, and to investigate whether physical exercise can improve coronary microvascular function. Hypotheses: The first hypothesis is that in INOCA, with reduced function of microvasculature of the heart, this reduced function also occurs in other organs of the body. The second hypothesis is that regular physical activity (aerobic exercise training) can improve coronary microvascular function, reduce symptoms, and that there is a parallel improvement in vascular function in other organs of the body.

Participants needed: 100
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Bispebjerg HospitalUpdated: Feb 21, 2025Locations: 2
Eligibility criteria

Coronary microvascular dysfunction, defined as myocardial bloodflow reserve (MBF... [+1]

Females of childbearing potential (defined as a premeno-pausal female capable of... [+6]

Status: Recruiting

Qishenyiqi Dripping Pill for Coronary Microvascular Disease

To investigate the efficacy and safety of Qishenyiqi in patients with microvascular angina pectoris. Long-term follow-up of 1 year will be performed to evaluate the effect of Qishenyiqi on coronary flow reserve and adverse cardiovascular events in patients with coronary microvascular disease.

Participants needed: 162
Trial details
Phase: Phase 4Age: 40-75Biological sex: AllType: InterventionalSponsor: Qilu Hospital of Shandong UniversityUpdated: Nov 21, 2024Locations: 3
Eligibility criteria

Repeated chest pain attacks with typical exertional angina pectoris or resting a... [+4]

Previous myocardial infarction or PCI or CABG treatment; [+9]

Status: Recruiting

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

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

Participants needed: 1,000
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Johannes Gutenberg University MainzUpdated: Nov 1, 2024Locations: 1Duration: 1 Year
Eligibility criteria

Patients who underwent combined measurements of coronary pressure and flow in at...

Hemodynamic instability [+1]

Status: Recruiting

Insulin Resistance and Coronary Microvascular Dysfunction in Patients with Myocardial Ischemia and Non-obstructive Coronary Artery Disease

The goal of this prospective study is to assess the correlation between coronary microvascular disfunction and insulin resistance in patients with INOCA. Patients with ANOCA and without diabetes will undergo invasive coronary microvascular assessment through coronary angiography and insulin resistance assessment through hyperinsulinemic-euglycemic clamp test. Patients enrolled in the study will be followed for a period of 2 years to monitor their clinical status.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Azienda Ospedaliera Universitaria Integrata VeronaUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

Aged over 18 years. [+2]

Obstructive CAD (defined as more than 70% luminal stenosis and/or FFR ≤0.80 in 1... [+7]

Status: Recruiting

Personalized Medicine Using Coronary Microvascular Function Measured in Patient With Percutaneous Coronary Intervention in Angina

The evidence demonstrating the importance of coronary microcirculation in the management of patients with coronary artery disease is growing. For example, in recent years, a number of studies have demonstrated that the presence of coronary microvascular disease (CMVD) contributes to increased cardiovascular morbidity and mortality independent of the extent and severity of coronary epicardial disease. The index of microcirculatory resistance (IMR) is an invasive index proposed for the diagnosis of CMVD. The ability of IMR to motivate therapeutic changes in order to subsequently reduce symptoms and improves the quality of life of our patients with stable coronary artery disease (CAD) was recently demonstrated. The prognostic value of IMR has also been shown in stable CAD with PCI. Thus, after optimal epicardial evaluation and if necessary revascularization according to FFR, IMR could represent a tool for personalized medicine adapted to the presence of severe CMVD. The aim of the study is to demonstrate a positive effect of personalized medicine on angina in patients with epicardial coronary network lesion assessment by FFR and with significant CMVD assessed by IMR.

Participants needed: 280
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, GrenobleUpdated: Jun 24, 2024Locations: 1
Eligibility criteria

Patient over 18 years [+5]

A non-coronary indication for coronary angiography, e.g. valve disease, hypertro... [+6]

Status: Recruiting

COSIMA: COronary SInus Reducer for the Treatment of Refractory Microvascular Angina

Patients with refractory microvascular angina fulfilling the predefined inclusion and exclusion criteria will be enrolled in this randomized trial. The primary objective is to investigate whether the proportion of patients reporting an improvement in Canadian Cardiovascular Society (CCS) angina class (≥2 classes) is different at six months after implantation of a Coronary Sinus Reducer followed by optimal medical therapy (OMT) compared to OMT alone.

Participants needed: 144
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Johannes Gutenberg University MainzUpdated: Sep 28, 2023Locations: 1
Eligibility criteria

Age ≥ 18 and ≤85 years [+5]

Recent (within 3 months) acute coronary syndrome [+18]