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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02762539
Other study ID # Omega 3 head injury
Secondary ID
Status Recruiting
Phase N/A
First received May 3, 2016
Last updated November 25, 2017
Start date June 2016
Est. completion date January 2018

Study information

Verified date November 2017
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Traumatic brain injury (TBI) is major health problem that stands as a significant cause of death and permanent disability. TBI is considered as global public health epidemic. On pathophysiologic basis, TBI is described as occurring in two phases, primary and secondary. Once a primary insult occurs like trauma or ischemia, the secondary injury begins though main four mechanisms; ischemia, brain edema, axonal injury and neuro-inflammation. Omega-3 PUFAs (Polyunsaturated fatty acids) are postulated to have neuroregenerative properties with the ability to impact all four main mechanisms of the secondary injury Patients will be allocated into one of two groups through a random table generation; Control group in which patients will follow our local protocol for TBI management without SMOF-lipid infusion. SMOF-lipid group in which patients will receive 0.5 g/Kg SMOF lipid 10% emulsion (Lipid emulsion for intravenous nutrition containing; 6% soybean oil / 6% medium chain triglycerides / 5% olive oil / 3%fish oil) daily over 12 hours starting once admitted to ICU for 7 days


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- mild to moderate head trauma

Exclusion Criteria:

- sensitivity to SMOF lipid severe head trauama

Study Design


Intervention

Drug:
omega-3 enriched SMOF lipid emusion


Locations

Country Name City State
Egypt Mansoura university Al Mansurah Dkahleya

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Glasgow coma scale after 48 hour of infusion 48 hours
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