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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03549481
Other study ID # 3 SH research
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 9, 2018
Est. completion date January 2019

Study information

Verified date August 2018
Source Benha University
Contact shaimaa A Mostafa, MD
Phone 01229122843
Email shaimaamustafa2011@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

role of different risk scores in acute coronary syndrome to predict left ventricular remodeling


Description:

patients with acute coronary syndrome (STEMI, NSTEMI, UA) will be included and different risk scores will be calculated for each patient.

after that in-hospital and short-term outcome beside left ventricular systolic and diastolic functions (at admission and 3m later) will be assessed to be correlated with different risk scores to determine which score system was able to predict left ventricular remodeling and what was the cut off value, sensitivity, and specificity of the score


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date January 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- patients with acute coronary syndrome

Exclusion Criteria:

- previous acute coronary syndrome previous PCI or CABG chronic renal disease decompensated liver disease patient refusal to participate patients dropped during follow up

Study Design


Locations

Country Name City State
Egypt shaimaa Mostafa Cairo

Sponsors (1)

Lead Sponsor Collaborator
shaimaa Mostafa

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary left ventricular remodeling end diastolic volume, end systolic volume, ejection fraction 3 months
Primary in hospital and short term outcme re-infarction, death, arrhythmia 3 months
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