- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05677503
Determination of the Red Cell Distribution Width, NT-proBNP and cTnT in Acute Myocardial Infarction Patients
Determination of the Relationship Between Red Cell Distribution Width, NT-proBNP and cTnT in Acute Myocardial Infarction Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patients and methods:
- Type of study: Observational prospective study
- Place of study: Sohag cardiology and gastroenterology center, department of cardiology and cardiac care unit.
- Ethical considerations: This research will be revised by the Scientific Ethical Committee of Sohag University Hospital. Consents will be taken from all patients.
Study Methods:
A prospective study on 30 patients diagnosed as acute myocardial infarction on which measurement of CBC, serum NT-proBNP, and cTnT levels will be performed at the time of admission and by the time of discharge.
Full history:
- Personal history: e.g. age, sex and smoking.
- Family history of cardiac diseases
- Medical history of: Hypertension, Ischemic heart disease, prior coronary artery bypass grafting, Prior Percutaneous coronary intervention, Prior Stroke, Prior Atrial fibrillation, therapeutic history
- Detailed clinical examination
- Electrocardiogram
Laboratory investigation:
- Routine investigation in the form of CBC including RDW
- Specific investigation which include NT-proBNP and cTnT
Study Type
Enrollment (Anticipated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
_All patients included in the study will be subjected to:
Full history:
- Personal history: e.g. age, sex and smoking.
- Family history of cardiac diseases
- Medical history of: Hypertension, Ischemic heart disease, prior coronary artery bypass grafting, Prior Percutaneous coronary intervention, Prior Stroke, Prior Atrial fibrillation, therapeutic history
- Detailed clinical examination
- Electrocardiogram
Laboratory investigation:
- Routine investigation in the form of CBC including RDW
- Specific investigation which include NT-proBNP and cTnT
Description
Inclusion Criteria:
- patients diagnosed as acute myocardial infarction
Exclusion Criteria:
Patient with
- Decompensated heart failure
- Pulmonary hypertention
- Acute pulmonary embolism
- Septic shock
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
complete blood count (CBC)
Time Frame: 7 months
|
measurement of CBC levels will be performed
|
7 months
|
Level of (NT-proBNP)
Time Frame: 7 months
|
measurement of serum NT-proBNP level will be performed
|
7 months
|
Level of (cTnT)
Time Frame: 7 months
|
measurement of cTnT level will be performed
|
7 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Sohag_Med_22_12_07
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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