Myocardial Infarction Clinical Trial
— MIMS3Official title:
Mental Stress and Myocardial Ischemia After MI: Sex Differences, Mechanisms and Prognosis
Verified date | January 2024 |
Source | Emory University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to look at the link between emotional stress and heart disease in men and women. Taking part in this study involves one clinic visit, one week of at home monitoring, and follow up phone calls every 6 months for 3 years.
Status | Enrolling by invitation |
Enrollment | 310 |
Est. completion date | June 2024 |
Est. primary completion date | June 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - History of documented MI within the past 8 months - Age =60 at the time of MI Exclusion Criteria: - History of unstable angina, MI, or decompensated heart failure in the past month - Patients deemed to be unsafe to hold anti-ischemic medications before testing (it is standard protocol to hold these meds before imaging studies) - Systolic blood pressure (SBP) >180 mm Hg or diastolic blood pressure (DBP) >110 mm Hg on the day of the test - Alcohol or substance abuse (past year), or severe psychiatric disorder other than major depression - Other serious medical disorders that may interfere with the study results - Postmenopausal hormone therapy (past 3 months) - Current psychotropic medications (past month) except anti-depressants - Pregnancy or breastfeeding (all women will receive a pregnancy test) - Severe aortic stenosis - Weight = 360 pounds and/or body mass index (BMI) of 40 or greater (weight limit of the SPECT imaging table) |
Country | Name | City | State |
---|---|---|---|
United States | Emory University Hospital | Atlanta | Georgia |
United States | Grady Health System | Atlanta | Georgia |
United States | The Emory Clinic | Atlanta | Georgia |
Lead Sponsor | Collaborator |
---|---|
Emory University | National Heart, Lung, and Blood Institute (NHLBI) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cardiovascular Events | The main outcome will be a composite endpoint of recurrent MI, unstable angina, hospitalization for decompensated heart failure, and cardiovascular (CV) death. A mental stress-induced myocardial ischemia (MSI) status of positive or negative will be the main predictor in regression models. | 3 Years | |
Secondary | Myocardial Infarction or Cardiovascular Death | The number of participants experiencing myocardial infarction or CV death in relation to MSI status (positive or negative). | 3 Years | |
Secondary | Cardiovascular Death | The number of participants experiencing CV death in relation to MSI status (positive or negative). | 3 Years | |
Secondary | Total Mortality | The number of participants experiencing all-cause death in relation to MSI status (positive or negative). | 3 Years | |
Secondary | Cardiovascular Events Excluding Heart Failure | This is a composite endpoint of recurrent MI, unstable angina, or CV death where the number of participants experiencing this endpoint in relation to MSI status (positive or negative) will be examined. | 3 Years |
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