EUCTR2004-001086-17-GB
Active, not recruiting
Not Applicable
Prospective randomised clinical trial to assess the efficacy of 70% v/v isopropyl alcohol and 2% w/v chlorhexidine in 70% v/v isopyl alcohol for the disinfection of skin prior to peripheral venous catheterisation. - Microbial contamination associated with ChloraPrep®
Medi-Flex0 sites900 target enrollmentJune 27, 2005
DrugsChloraPrep:
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Medi-Flex
- Enrollment
- 900
- Status
- Active, not recruiting
- Last Updated
- 12 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient and healthcare worker inclusion criteria
- •\-Must be at least 18 years of age.
- •\-Require a PVC as part of their clinical management.
- •\-Willing and able to provide verbal consent.
- •Healthcare worker
- •\-Competent to insert PVC as part of their clinical practice.
- •\-Completion of the study training programme.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
Exclusion Criteria
- •Patient and healthcare worker exclusion criteria
- •Any patient may withdraw from the study at their own request for any reason, or at the request of their medical team, the Clinical Research Nurse, the Principal Investigator or in the case of an adverse event. History of psychiatric problems or mental handicap, breast feeding and pregnant women, anyone less than 18 years of age, patients unable to give informed consent.
- •Healthcare worker
- •Any healthcare worker may withdraw from the study at their own request for any reason, or at the request of the Clinical Research Nurse or Principal Investigator.
Outcomes
Primary Outcomes
Not specified
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