Cardiovascular Diseases Clinical Trial
To determine if intermittent ST depression (STD) had an independent impact on survival among myocardial infarction patients who participated in the Beta-Blocker Heart Attack Trial (BHAT).
BACKGROUND:
In 1988, coronary heart disease was the leading cause of death in the United States,
accounting for some 500,000 lives annually. The search continued for non-invasive ways of
improving risk-detection in the population prior to and after manifest disease. Detection of
silent ischemia, as indicated by the presence of asymptomatic intermittent ST depression
detected by ECG monitoring, was accomplished by non-invasive means and data analysis was
determined with current, automated analysis programs. However, there were insufficient data
to assign definite prognostic import to intermittent STD. The studies addressing this
question were in selected populations and yielded conflicting results. This was in part due
to the small size of the populations previously studied. The size of this study's population
permitted examination of additional criteria for ST changes in relation to prognosis. A
finding that transient ischemia adversely affected prognosis in a large group of patients
who had myocardial infarction would therefore give confidence to the medical community in an
accessible non-invasive technique to identify those at highest risk. This would have an
important impact on patient management. Impetus would also be given toward studying
asymptomatic STD among high risk patients (hypertensives, hypercholesterolemics, smokers,
and diabetics) without clinical coronary heart disease to determine if its presence
increased the risk of developing myocardial infarction or sudden death.
The BHAT trial was a double-blind, randomized trial of the effects of propranolol on
survival after acute myocardial infarction. The total group numbered 3,837 patients, aged
30-69. Patients were excluded from the study if they had medical contraindications to
propranolol, a history of severe congestive heart failure or asthma as an adult, or if they
had or were likely to undergo cardiac surgery. Clinical and personal characteristics and ECG
data, including the results of 24-hour monitoring from the baseline reference examination,
were completed while patients were hospitalized prior to randomization. Patients were seen
at regular intervals and a random sample of 1,000 patients had a second 24-hour monitoring
at 6 weeks. Also at this visit, a psychosocial stress questionnaire was completed for 2,320
men. Patients were followed for a minimum of one and up to three years after index
myocardial infarction. Official follow-up was terminated at 3 years on the recommendation of
the Policy Monitoring Board. The main finding of improved survival among patients taking
propranolol has been widely reported.
DESIGN NARRATIVE:
This was a case-control study. The main issue examined was whether intermittent STD
contributed significantly to mortality when other prognostic variables such as prior
myocardial infarction, heart failure, arrhythmia, and diabetes were simultaneously
controlled for. Using BHAT computer and ECG tapes, 326 deaths observed during the BHAT
follow up were compared to 326 controls.
Substudy I examined the joint impact of psychosocial stress and intermittent STD on survival
utilizing records of 200 cases or deaths and 200 controls who had the psychosocial stress
interview in the BHAT.
Substudy II examined whether propranolol had a favorable impact on STD status from baseline
to repeat examination. The design of this substudy was prospective. One hundred fifty
patients treated with propranolol and 150 untreated controls were randomly selected from
among the 1,000 patients who had repeat 24-hour Holter monitoring at the six week follow-up
visit. Patients were followed from baseline to repeat monitoring at six weeks with the STD
durations at baseline and repeat monitoring being followed for each patient.
An univariate substudy examined the prevalence of STD in approximately 180 patients from the
substudy II cohort who had completed a psychosocial stress interview in order to determine
if elevated psychosocial stress was associated with STD. A second univariate substudy
examined the effect of diabetes on the prevalence of STD. A third univariate substudy
examined the effect of STD on the prevalence of arrhythmia.
Dr. Richard Crow at the University of Minnesota was responsible for the reading of the
24-hour Holter tapes. Computer analyses were done at Dalhousie University, Halifax, Nova
Scotia, Canada.
;
N/A
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05650307 -
CV Imaging of Metabolic Interventions
|
||
| Recruiting |
NCT05654272 -
Development of CIRC Technologies
|
||
| Recruiting |
NCT04515303 -
Digital Intervention Participation in DASH
|
||
| Completed |
NCT04056208 -
Pistachios Blood Sugar Control, Heart and Gut Health
|
Phase 2 | |
| Recruiting |
NCT04417387 -
The Genetics and Vascular Health Check Study (GENVASC) Aims to Help Determine Whether Gathering Genetic Information Can Improve the Prediction of Risk of Coronary Artery Disease (CAD)
|
||
| Not yet recruiting |
NCT06211361 -
Cardiac Rehabilitation Program in Patients With Cardiovascular Disease
|
N/A | |
| Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
| Recruiting |
NCT04514445 -
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
|
||
| Enrolling by invitation |
NCT04253054 -
Chinese Multi-provincial Cohort Study-Beijing Project
|
||
| Completed |
NCT03273972 -
INvestigating the Lowest Threshold of Vascular bENefits From LDL Lowering With a PCSK9 InhibiTor in healthY Volunteers
|
N/A | |
| Completed |
NCT03680638 -
The Effect of Antioxidants on Skin Blood Flow During Local Heating
|
Phase 1 | |
| Recruiting |
NCT04843891 -
Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis.
|
Phase 1 | |
| Completed |
NCT04083872 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of Highdose CKD-385 in Healthy Volunteers(Fasting)
|
Phase 1 | |
| Completed |
NCT04083846 -
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers(Fed)
|
Phase 1 | |
| Completed |
NCT03619148 -
The Incidence of Respiratory Symptoms Associated With the Use of HFNO
|
N/A | |
| Completed |
NCT03693365 -
Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial
|
||
| Completed |
NCT03466333 -
Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia
|
Phase 2 | |
| Completed |
NCT04082585 -
Total Health Improvement Program Research Project
|
||
| Completed |
NCT05132998 -
Impact of a Comprehensive Cardiac Rehabilitation Program Framework Among High Cardiovascular Risk Cancer Survivors
|
N/A | |
| Completed |
NCT05067114 -
Solutions for Atrial Fibrillation Edvocacy (SAFE)
|