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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04228510
Other study ID # 2DSE
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2020
Est. completion date December 2021

Study information

Verified date January 2020
Source Assiut University
Contact Aly Tohamy, MD
Phone 01006258877
Email Ali.tohamy@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

ST-segment elevation myocardial infarction (STEMI) is a major cause of morbidity and mortality worldwide. In spite of decrease in acute and long-term mortality following STEMI in parallel with more use of reperfusion therapy, such as primary percutaneous coronary intervention (PPCI), modern antithrombotic therapy, and secondary prevention, mortality remains considerable. Reduced EF is a well-known predictor of increased short and long term major adverse cardiovascular events MACE :( heart failure, stroke and death)


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 204
Est. completion date December 2021
Est. primary completion date September 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- ST elevation myocardial infarction patients after primary percutaneous coronary intervention

Exclusion Criteria:

- Previous myocardial infarction.

- Sever or haemodynamically significant (associated with chamber dilation) valvular heart diseases.

- Previous heart failure.

- Previous cerebrovascular strokes.

- Atrial fibrillation.

- Severe comorbidities as severe renal impairment, hepatic or respiratory failure.

- Bad equality views which affects accurate speckle tracking imaging.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
2D speckle tracking echocardiography
Global and segmental strain and strain rate in longitudinal and circumferential directions will be detected after PPCI; before discharge. The LV circumferential strains and strain rates will be determined from the short-axis views at the basal, middle, and apical levels, and longitudinal strains and strain rates will be determined from the apical 2-, 3-, and 4-chamber views of the LV. Segmental longitudinal strains equal to -15% or closer to 0 will be considered abnormal (injured segments). The average segmental longitudinal strain and strain rate of the abnormal segments is defined as the injury longitudinal strain (InjLS) and injury longitudinal systolic strain rate (InjLSRs).

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary The Incidence of major adverse cardiovascular events the rate of Acute coronary syndrome, Heart failure, Stroke and all-cause mortality 1 year
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