MiVa: Characterization of Different Phenotypes of Microvascular Dysfunction and Their Impact on Angina Severity in Patients With Chronic Angina in the Absence of Obstructive Coronary Artery Disease.

Sponsor
Federico II University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05686707
Collaborator
University of Catanzaro (Other)
400
1
60.5
6.6

Study Details

Study Description

Brief Summary

The aim of the present study will be to identify different phenotypes of microvascular dysfunction and their associations with the severity of anginal symptoms assessed through the Seattle Angina Questionnaire(SAQ-7).

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    After administration of unfractionated heparin (100UI/Kg), a special pressure guide (Pressure Wire X, Abbott), equipped with a distal sensor capable of measuring pressure and temperature, will be introduced inside the anterior descending branch (IVA) of the left coronary artery and hyperemia will be induced by intravenous infusion of adenosine. The IMR will be calculated using the thermodilution technique, and is given by the product between the mean distal pressure, in the left anterior descending coronary artery, and the mean transit time (Tmn) during maximal hyperemia.

    During the procedure, additional coronary physiological indices will be calculated such as:
    • Quiescent full cycle flow ratio (RFR), - Fractional flow reserve (FFR),

    • Coronary flow reserve (CFR)

    In order to identify different phenotypes of microvascular dysfunction, as follows:
    • Phenotype A: Patients with IMR>25, CFR <2 and FFR>0.80 (concordant pure-microvascular pathological results)

    • Phenotype B: patients with IMR>25, CFR>2 and FFR>0.80 (increased microvascular hyperemic resistance, maintenance of microvascular reactivity)

    • Phenotype C: Patients with IMR 25, CFR 2 and FFR>0.80 (normal hyperemic resistance and reduced reactivity) All these phenotypes can also be combined with pathological FFR measures (<0.80) (phenotypes A1, B1, C1).

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    400 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Characterization of Different Phenotypes of Microvascular Dysfunction and Their Impact on Angina Severity in Patients With Chronic Angina in the Absence of Obstructive Coronary Artery Disease
    Actual Study Start Date :
    Jul 18, 2022
    Anticipated Primary Completion Date :
    Aug 1, 2023
    Anticipated Study Completion Date :
    Aug 1, 2027

    Outcome Measures

    Primary Outcome Measures

    1. (SAQ-7) [12 months]

      Identify different phenotypes of microvascular dysfunction and their associations with anginal symptom severity assessed through the Seattle Angina Questionnaire (SAQ-7).

    Secondary Outcome Measures

    1. characterization of the severity of angina [12 months]

      To validate the ability of the microvascular resistance index to identify patients who have microvascular disease and its utility in characterizing angina severity. Identify different phenotypes of microvascular dysfunction and their associations with comorbidities, cardiovascular risk factors, and drug therapy. A sub-analysis on the use of different antianginal drugs will be performed to better understand the impact of pharmacotherapy on different microvascular dysfunction phenotypes. Evaluate the health status of patients in different microvascular dysfunction phenotypes through the EQ-5D-5L questionnaire. EQ-5D is a standardized measure of health status developed by the EuroQoL Group in order to provide a simple and generic measure of health for clinical and economic evaluation. Evaluate the state of depression induced by the disease through "The Brief Illness Perception Questionnaire (B-IPQ).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    Patients who meet all of the following criteria will be considered for study participation:

    Age ≥18 and <85 years. Chronic coronary syndrome (including patients with anginal equivalents) Angina CCS class II-IV Evidence of inducible reversible ischemia in noninvasive trials

    Availability of the following measurements:
    • Microvascular resistance index (IMR)

    • Quiescent full cycle flow ratio (RFR),

    • fractional flow reserve (FFR),

    • Coronary flow reserve (CFR) Willingness to participate and sign the informed consent document prior to the procedure.

    Exclusion Criteria:
    At least one of the following:

    Pregnancy or breastfeeding. Medical or psychological conditions that would compromise proper and orderly participation.

    Left ejection fraction less than 30% Prior coronary artery bypass surgery (CABG) Decompensated congestive heart failure (CHF) Chronic or acute renal failure with creatinine

    2mg/dl Severe valve disease Patients with comorbidities limiting life expectancy to less than one year.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Federico II University of Naples Naples Italy 80131

    Sponsors and Collaborators

    • Federico II University
    • University of Catanzaro

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Giovanni Esposito, Full Professor, Federico II University
    ClinicalTrials.gov Identifier:
    NCT05686707
    Other Study ID Numbers:
    • 333-21
    First Posted:
    Jan 17, 2023
    Last Update Posted:
    Jan 17, 2023
    Last Verified:
    Jan 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Giovanni Esposito, Full Professor, Federico II University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 17, 2023