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Assessing the effect of vitamin B1 and vitamin C on treatment of sever sepsis

Phase 3
Recruiting
Conditions
sepsis.
Other sepsis
Registration Number
IRCT20210518051339N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
86
Inclusion Criteria

presence of sever sepsis based on the diagnosis of expert doctor of infectious diseases
the age up of 18
the patient or his accompany can give Informed consent

Exclusion Criteria

allergic reaction to vitamin B1 and vitamin C
patients can exit from study with their tendency

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measure of mortality. Timepoint: 4 days after beginning of consumption of B1 and C vitamines. Method of measurement: report of doctor.
Secondary Outcome Measures
NameTimeMethod
Recovery. Timepoint: 4 days after consumption of B1 and C vitamines. Method of measurement: report of doctor.;Duration of hospitalization. Timepoint: 4 days after consumption of B1 and C vitamines. Method of measurement: report of doctor.
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