Targeted medical therapy for angina with non-obstructive coronary arteries
Official title: A Randomized Controlled Study of Targeted Medical Therapy Versus Placebo for Angina and Non- Obstructive Coronary Arteries: The MVP-ANOCA Study
Run by Stanford University · NCT06424834 · Data updated 2026-11-12
This study is testing if a new targeted medication can help people with angina and non-obstructive coronary arteries feel better and improve their quality of life.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Stanford University Academic / other |
| Locations | 1 site (Palo Alto, California) |
| Status | Recruiting |
| Started | October 10, 2024 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | November 27, 2024 |
| Trial ID | NCT06424834 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients with stable angina who have undergone coronary function testing and have been diagnosed with specific conditions related to non-obstructive coronary arteries.
✕Probably not a fit
Patients with acute coronary syndrome, significant epicardial coronary artery disease, or contraindications to the study medications may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial aims to evaluate the effectiveness of targeted medical therapy in improving symptoms and quality of life for patients suffering from angina and non-obstructive coronary arteries. Participants will receive either active medication or a placebo for a duration of four weeks, following a drug titration phase. The study will assess the impact of these treatments through questionnaires measuring quality of life before and after the intervention, after confirming the cause of chest pain through coronary function testing.
Why it matters
Potential benefit: If successful, this study could provide a new treatment option that significantly alleviates symptoms for patients with angina and non-obstructive coronary arteries.
How similar studies have gone: While there have been studies on angina treatments, this specific approach targeting non-obstructive coronary arteries is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * All patients with stable angina referred to the Stanford University Hospital cardiac catheterization laboratory for clinically indicated coronary function testing are eligible for inclusion into the study. Specific inclusion criteria for randomization: * Absence of significant epicardial coronary artery disease on angiography * Fractional flow reserve \> 0.80 And ≥ 1 of the following: * Epicardial coronary spasm on acetylcholine testing * Microvascular spasm on acetylcholine testing * Coronary flow reserve \< 2.5 * Index of microcirculatory resistance ≥ 25 * Myocardial bridge on intravascular ultrasound with dobutamine resting full-cycle ratio ≤ 0.76 Exclusion Criteria: * Acute coronary syndrome less than one week prior to enrolment * Cardiomyopathy * Contraindications to beta-blockers or calcium channel blockers * Baseline systolic blood pressure \< 95 mmHg * Baseline heart rate \< 55 bpm
Where it's running
-
Stanford Hospital
Palo Alto, California, United States Recruiting
Study contacts
- Principal investigator: Jennifer Tremmel, MD — Stanford University
- Study coordinator: Christopher Wong, MBBS, PhD
- Email: ccywong@stanford.edu
- Phone: (650) 725 5909
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.