- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06718374
Chest Pain Symptoms Differences Between Diabetic Patients and Non (chestpaindm)
Chest Pain Symptoms Differences Between Diabetes Mellitus and Non-diabetes Mellitus Patients with Acute Coronary Syndrome
Study Overview
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Antonios S Ishak, Resident
- Phone Number: 20 1226366806
- Email: tonysamir993@gmail.com
Study Contact Backup
- Name: Antonios S Ishak, Resident
- Phone Number: 01226366806
Study Locations
-
-
-
Assiut, Egypt, 2063045
- Recruiting
- Assiut University
-
Contact:
- Antonios S Ishak, Resident
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
i) Patients diagnosed with STEMI and NSTEMI ii) Both genders iii) above the age of 30 years iv) Patients with acute myocardial infarction with or without chest pain (angina) for 24 hours v) patients who are hemodynamically stable vi) patients without acute decompensated heart failure (ADHF) vii) patients without malignant arrhythmias viii) patients without in Acute Lung Oedem (ALO) condition ix) patients not using ventilator x) patient willing to and become respondents.
Exclusion Criteria:
i) Patients with several complications, thereby making it impossible to interview them ii) patients who have never undergone CABG surgery iii) patients who refuse to be respondents
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
non diabetic
|
Ecg detection for nstemi and stemi in diabetic and non diabetic paturnts
Other Names:
|
|
diabetic
|
Ecg detection for nstemi and stemi in diabetic and non diabetic paturnts
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Mortality
Time Frame: One month
|
One month
|
|
Hospital admission
Time Frame: 1 day
|
1 day
|
|
Intensive Care Unit admission
Time Frame: One week
|
One week
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Essam El-dien M Abdullah, MD, Assiut University
- Study Director: Zeinab Abd-Elatiff, MD, Ismailia Universiry
- Study Director: Khalid Abdelbaky, MD, Assiut University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- chestpain
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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