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

S

Sohag University

Status

Not yet enrolling

Conditions

Myocardial Infarction

Treatments

Diagnostic Test: (cTnT)
Diagnostic Test: CBC
Diagnostic Test: (NT-proBNP)

Study type

Observational

Funder types

Other

Identifiers

NCT05677503
Sohag_Med_22_12_07

Details and patient eligibility

About

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.

Full 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

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients diagnosed as acute myocardial infarction

Exclusion criteria

Patient with

  • Decompensated heart failure
  • Pulmonary hypertention
  • Acute pulmonary embolism
  • Septic shock

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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