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Effect of curcumin on systemic inflammatory response syndrome

Phase 3
Recruiting
Conditions
sepsis/at risk of sepsis.
Systemic inflammatory response syndrome (SIRS) of non-infectious origin
Registration Number
IRCT20110123005670N27
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Critically ill patients with APACHE II score of 15-30
Positive SIRS
Age over 18 and under 60
At least 10 days hospitalization in ICU
Patients who received enteral nutrition formula

Exclusion Criteria

Parenteral feeding
Enteral nutrition and gavage formula intolerance
Patients expected to die within the next 24 hours
HIV positive patients
Pregnant and lactating women
ileus
Immune disorder
Diabetes melitus
Short bowel syndrome
Pancreatitis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Protein C. Timepoint: Day 1, 5 and 10 of intervention. Method of measurement: ELISA Kit.;Partial Thromboplastin time. Timepoint: Day 1, 5 and 10 of intervention. Method of measurement: ELISA kit.;Prediction of death. Timepoint: Day 1, 5 and 10 of intervention. Method of measurement: Simplified Acute Physiology Score questionnaire.;Transforming growth factor ß1. Timepoint: Day 1, 5 and 10 of intervention. Method of measurement: ELISA kit.
Secondary Outcome Measures
NameTimeMethod
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