Actively Recruiting
Chest Pain Symptoms Differences Between Diabetes Mellitus and Non-diabetes Mellitus Patients with Acute Coronary Syndrome
Led by Assiut University · Updated on 2024-12-06
50
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Cardiovascular disease is the leading cause of death among non-infectious diseases, responsible for 17.5 million deaths worldwide. This research investigates differences in chest pain symptoms between patients with diabetes mellitus and those without, focusing on acute coronary syndrome. The study explores how silent ischemia, often linked to autonomic neuropathy in diabetic patients, affects their experience of chest pain. The study observes patients diagnosed with ST-elevation myocardial infarction (STEMI) and non-ST-elevation myocardial infarction (NSTEMI). Participants include both diabetic and non-diabetic individuals who have had an acute myocardial infarction with or without chest pain within the past 24 hours. The study monitors hospital admissions, intensive care unit admissions within one week, and mortality within one month. Participants will be evaluated while hemodynamically stable and free from acute decompensated heart failure, malignant arrhythmias, acute lung edema, and ventilator use. Researchers will collect clinical data to compare chest pain symptoms and outcomes between diabetic and non-diabetic groups. The total participation duration includes immediate hospital care and follow-up for one month to assess key health outcomes and survival.
CONDITIONS
Brief Title
Chest Pain Symptoms Differences Between Diabetic Patients and Non
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with STEMI and NSTEMI
- Both genders
- Above the age of 30 years
- Patients with acute myocardial infarction with or without chest pain (angina) for 24 hours
- Patients who are hemodynamically stable
- Patients without acute decompensated heart failure (ADHF)
- Patients without malignant arrhythmias
- Patients without Acute Lung Oedema (ALO) condition
- Patients not using ventilator
- Patient willing to and become respondents
You will not qualify if you...
- Patients with several complications, making it impossible to interview them
- Patients who have never undergone CABG surgery
- Patients who refuse to be respondents
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 month
Participants are observed to track hospital admission, intensive care unit admission, and mortality outcomes following acute coronary syndrome.
Visits as needed during hospital stay and follow-up over 1 month
Trial Site Locations
Total: 1 location
1
Assiut university
Asyut, Asyut Governorate, Egypt, 2063045
Actively Recruiting
Research Team
A
Antonios S Ishak, Resident
A
Antonios S Ishak, Resident
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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