The effect of curcumin on septic patients

Phase 2

Recruiting

• Conditions: sepsis.; Sepsis with septicemia; A41.9

• Registration Number: IRCT20211023052849N2
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 4 April 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

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Exclusion Criteria

entral feeding intolerance
estimation of death in next 24 hours
pregnancy and breast feeding
systolic blood pressure less than 90 mm-Hg resistant to therapy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ength of stay in ICU. Timepoint: daily. Method of measurement: patient documents.

Secondary Outcome Measures

Name	Time	Method
TNF-alpha. Timepoint: 0, 5 days after intervention. Method of measurement: ELISA.;IL-6. Timepoint: 0, 5 days after intervention. Method of measurement: ELISA.;ESR. Timepoint: 0, 5 days after intervention. Method of measurement: ELISA.;Crp. Timepoint: 0, 5 days after intervention. Method of measurement: ELISA.;CBC. Timepoint: 0, 5 days after intervention. Method of measurement: -.