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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04408612
Other study ID # 01-05/20
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 6, 2020
Est. completion date November 1, 2023

Study information

Verified date November 2023
Source National Medical Research Center for Therapy and Preventive Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Single-centre prospective study to characterize causes of dyspnea in stable patients with coronary artery disease and evaluate the possibility to determine the cause of dyspnea before in-depth examination.


Description:

Stable patients with dyspnea and coronary artery disease will be included in this single-centre prospective study. In addition to routine clinical examination patients will be interviewed to determine the nature of shortness of breath, angina, presence of chronic heart failure or anxiety using the Medical Research Council Dyspnea scale, the visual analog scale of dyspnea, Borg scale, modified "dictionary" of dyspnea, G. Rose questionnaire, Seattle Angina Questionnaire, Framingham criteria for chronic heart failure and the SHOCK scale. During the subsequent in-depth examination including thyroid hormones, NT-proBNP, hsTroponin, ECG monitoring, six-minute walk test, stress-echo with a diastolic stress test, spirometry and coronary angiography (if necessary) main reason for dyspnea will be established. Possibilities of early (before in-depth examination) determination the reason for dyspnea in stable patients with coronary artery disease will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date November 1, 2023
Est. primary completion date November 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Stable patients with shortness of breath and established diagnosis of coronary artery disease (at least 1 of the following signs): - history of myocardial infarction; - typical angina without suspected other cause of pain; - myocardial ischemia documented by ECG changes during symptoms and/or by results of the stress test; - coronary artery stenosis >50% according to coronary angiography. 2. Signed informed consent. Exclusion Criteria: 1. Acute coronary syndrome (myocardial infarction, unstable angina) in the previous month. 2. Hospitalization with decompensation of CHF in the previous 6 months (including CHF decompensation as the main reason for current hospitalization). 3. Diseases with an unfavourable prognosis (terminal CKD, CHF NYHA IV, a lung disease with severe respiratory failure). 4. Contraindications to bicycle stress echocardiography. 5. Atrial Fibrillation at the time of hospitalization, when the decision not to restore the sinus rhythm. 6. Mental illnesses and disorders, dementia, drug or alcohol dependence. 7. Known oncological diseases.

Study Design


Intervention

Diagnostic Test:
Scales for assessment of symptoms
Medical Research Council Dyspnea scale, the visual analogue scale of dyspnea, Borg scale, modified "dictionary" of dyspnea, G. Rose questionnaire, Seattle Angina Questionnaire, Framingham criteria for chronic heart failure, the SHOCK scale.

Locations

Country Name City State
Russian Federation National Research Centre for Therapy and Preventive Medicine Moscow

Sponsors (1)

Lead Sponsor Collaborator
National Research Center for Preventive Medicine

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary Myocardial ischemia as a reason of dyspnea Number of patient with dyspnea related to myocardial ischemia up to 1 month
Secondary Other causes of dyspnea Number of patient with non-ischemic reasons for dyspnea (heart failure, pulmonary disease, arrhythmias, psychogenic, mixed or undetermined cases). up to 1 month
Secondary Adverse events Composite of death, myocardial infarction, stroke and rehospitalization 6 months
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