Overview

Lipid Emulsion Infusion and COVID-19 Patients

Status:
Completed
Trial end date:
2021-09-26
Target enrollment:
0
Participant gender:
All
Summary
Investigators suggest that early administration of intravenous lipid emulsion (ILE) affect the inflammatory response and improve outcome in COVID-19. The aim of this trial is to study the effect of fish-oil-based intravenous lipid emulsion (FOBLE) supplementation added to enteral nutrition on shift to ICU for upgrading oxygenation &/or ventilation in moderate cases of Covid-19 diseased patients requiring only supplemental oxygen in form of simple nasal cannula or venturi mask oxygen (during 7 days admission).
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Assiut University
Treatments:
SMOFlipid
Criteria
Inclusion Criteria:

- Patients are with diagnosis of moderate cases of covid-19 (a person who may have lower
respiratory illness, such as pneumonia. However, their blood oxygen levels remain
≥94%)

- Requiring only supplemental oxygen in form of simple nasal cannula or venturi mask
oxygen admitted in the intermediate care attached to our ICU with good enteral
nutrition.

Exclusion Criteria:

- Hypersensitivity (peanut,eggs and soya bean)

- Uncontrolled hyperlipidemia

- Severe primary blood coagulation diseases

- Acute pancreatitis

- Acute thromboembolic diseases

- Liver failure (bilirubin >40 mmol/l, alanine aminotransferase >100 U/l and aspartate
aminotransferase >100 U/l)

- RIFLE (Risk, Injury, Failure, Loss of kidney function and End-stage kidney disease)
stage III and IV renal failure

- Pregnancy or lactation

- Severe neutropenia (<500 cells/mm3)