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NCT05677503 Clinical Trial

Determination of the Red Cell Distribution Width, NT-proBNP and cTnT in Acute Myocardial Infarction Patients

Myocardial Infarction Clinical Trial

Official title:
Determination of the Relationship Between Red Cell Distribution Width, NT-proBNP and cTnT in Acute Myocardial Infarction Patients

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05677503
Other study ID # Sohag_Med_22_12_07
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 15, 2023
Est. completion date July 30, 2023

Study information
Verified date January 2023
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

the study is to investigate the relationship of several parameters of complete blood count (CBC) including RDW with N-terminal pro-B-type natriuretic peptide (NT-proBNP) and cardiac troponin T (cTnT) in a cohort of acute myocardial infarction (AMI) patients.

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. 1. Full history: 1. Personal history: e.g. age, sex and smoking. 2. Family history of cardiac diseases 3. Medical history of: Hypertension, Ischemic heart disease, prior coronary artery bypass grafting, Prior Percutaneous coronary intervention, Prior Stroke, Prior Atrial fibrillation, therapeutic history 2. Detailed clinical examination 3. Electrocardiogram 4. Laboratory investigation: 1. Routine investigation in the form of CBC including RDW 2. Specific investigation which include NT-proBNP and cTnT

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date July 30, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - patients diagnosed as acute myocardial infarction Exclusion Criteria: Patient with - Decompensated heart failure - Pulmonary hypertention - Acute pulmonary embolism - Septic shock

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• CBC
measurement of CBC will be performed at the time of admission and by the time of discharge
• (NT-proBNP)
measurement of serum NT-proBNP levels will be performed at the time of admission and by the time of discharge
• (cTnT)
measurement of cTnT levels will be performed at the time of admission and by the time of discharge

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Sohag University

Outcome
Type Measure Description Time frame Safety issue
Primary complete blood count (CBC) measurement of CBC levels will be performed 7 months
Primary Level of (NT-proBNP) measurement of serum NT-proBNP level will be performed 7 months
Primary Level of (cTnT) measurement of cTnT level will be performed 7 months
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