Effect of soy protein Isolate and flaxseed oil in burn patients

Not Applicable

• Conditions: burn.; Burn of unspecified degree of trunk

• Registration Number: IRCT2014051817740N1
• Lead Sponsor: Vice Chancellor of Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 69

Inclusion Criteria

Inclusion Criterias : People aged15-60 years ; Willingness to cooperate ; People with body surface area between 20% -50% ; oral nutrition ; During peak of burn admissions 24-48 hours
Exclusion Criterias : Having an allergy to soy ; consumtion of omega-3 during the previous week or month ; having kidney disease(Dialysis),having liver disease ; Pregnant and lactating women ; Excessive hemorrhage ; Having a weight loss greater than 10% within 6 months prior to admission ; BMI(body mas index)<18, BMI>30 kg/m2 ; Failure to adhere to consume at least 80% of the number of cookies consumed during the study

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hs-CRP(high sensetive- C Reactive Protein). Timepoint: Before the intervention, and 21 days after intervention. Method of measurement: Elisa.;SOD(Super Oxide Dismutase). Timepoint: Before the intervention, and 21 days after intervention. Method of measurement: Spectrophotometric.;MDA(Malondialdehyde). Timepoint: Before the intervention, and 21 days after intervention. Method of measurement: Satoh method with thiobarbituric acid solution.

Secondary Outcome Measures

Name	Time	Method
Apparent Nitrogen balance. Timepoint: Before the intervention, and 21 days after intervention. Method of measurement: Spectrophotometric.;Total lymphocyte count. Timepoint: Before the intervention, and 21 days after intervention. Method of measurement: Spectrophotometric.;Ferritin. Timepoint: Before the intervention, and 21 days after intervention. Method of measurement: Elisa.