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Effect of MitoQ versus placebo on clinical outcomes in patients with early septic shock

Phase 3
Conditions
Early septic shock.
Severe sepsis with septic shock
R65.21
Registration Number
IRCT20120215009014N499
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
40
Inclusion Criteria

Age 18 to 65 years
Premature septic shock
Receive vasopressor for at least 6 and maximum for 24 hours

Exclusion Criteria

Pregnancy or breastfeeding
Treated with other antioxidant and anti-inflammatory drugs
Chronic liver or kidney disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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