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NCT04806425 Clinical Trial

The Cardioprotective Effect of Intralipid in Decreasing the Ischemic Insults During Off-pump Coronary Artery Revascularization

Anesthesia Clinical Trial

Official title:
The Cardioprotective Effect of Intralipid in Decreasing the Ischemic Insults During Off-pump Coronary Artery Revascularization

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04806425
Other study ID # FMASU R 126/2020
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date October 1, 2020
Est. completion date March 1, 2021

Study information
Verified date March 2021
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the aim of the study is to assess the effect of intralipid as regard efficiency in decreasing myocardial ischemia , given during preconditioning in off pump coronary artery revascularization

Recruitment information / eligibility
Status Completed
Enrollment 46
Est. completion date March 1, 2021
Est. primary completion date February 20, 2021
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria: - patients between 40 to 75 undergoing off bump CABG surgery Exclusion Criteria: - emergency surgery - Ejection fraction less than 50% - redo procedures - history of allergy to peanuts

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Intralipid
intralipid is given as a preconditioning drug during off bump coronary artery bypass grafting surgery to measure efficacy in decreasing post operative ischemia
• Placebo
normal saline is given in same volume to normal saline group over the same duration

Locations
Country Name City State
Egypt Ain Shams University Cairo (Select)

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary ICU stay measuring the duration of stay in the ICU long icu stay is considered if more than 7 days
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