Investigation for safety and efficacy of a new antiseptic Olanexidine Gluconate in childre
Not Applicable
- Conditions
- Patients who undergo surgery of catheter insertion or inguinal hernia
- Registration Number
- JPRN-UMIN000027899
- Lead Sponsor
- ational Center for Child Health and Development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 55
Inclusion Criteria
Not provided
Exclusion Criteria
(1)History of drug sensitivity. (2)History of shock or hypersensitivity against Chlorhexidine gluconate. (3)Patients having cutaneous disease (4)Any patients who was judged as inappropriate candidate to enroll this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome was determined to assess the rate of any adverse effect such as labo data, vital sign, subjective and objective symptom, erythema or irritation of the skin.
- Secondary Outcome Measures
Name Time Method