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Red Cell Distribution Width,,NT-proBNP and cTnT in Acute Myocardial Infraction Patient

Not yet recruiting
Conditions
Myocardial Infarction
Registration Number
NCT05595278
Lead Sponsor
Sohag University
Brief 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.

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.

* All patients included in the study will be subjected to:

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 & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • patients diagnosed as acute myocardial infarction and admitted to department of cardiology and cardiac care unit at Sohag cardiology and gastroenterology center according to inclusion and exclution criteria
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Exclusion Criteria

Patient with:

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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
(CBC)6 months

measurement of CBC will be performed at the time of admission and by the time of discharge.

(cTnT)6 months

measurement of cTnT levels will be performed at the time of admission and by the time of discharge

(NT-proBNP6 months

measurement of serum NT-proBNP levels will be performed at the time of admission and by the time of discharge.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sohag University Hospital

🇪🇬

Sohag, Egypt

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