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Efficacy and safety of olanexidine gluconate for skin disinfection of blood culture collectio

Phase 2
Recruiting
Conditions
Infections
Infections, Sepsis, Bacteremia
Registration Number
JPRN-jRCTs061220073
Lead Sponsor
Ota Kohei
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
215
Inclusion Criteria

1. over 18 years
2. Patients from whom blood culture was collected in the emergency department or the intensive care unit
3. Provision of written informed consent from patients or their surrogate

Exclusion Criteria

1. History of allergy or contact dermatitis caused by 1.5% oranexidine (for those who have already been enrolled in this study, including those who have been found to have adverse events in this study for which a causal relationship with 1.5% oranexidine cannot be denied.)
2. Patients with systemic skin diseases
3. Patients with wound or skin ulcer at the puncture site
4. Patients whose puncture site is contaminated with feces, urine, or sludge, and who require procedures other than disinfection such as wiping.
5. Patients who have received antimicrobial agents with antimicrobial activity against contaminating bacteria.

Study & Design

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