Controlling device Occlusion by needleless ConnectOr design. A pilot randomised control trial (COCOA Trial)
- Conditions
- Peripheral intravenous catheter failurePublic Health - Health service research
- Registration Number
- ACTRN12619001091190
- Lead Sponsor
- Griffith University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 200
1. Patient requires a PVC for greater than 24 hours
2. PVC has not been insitu greater than 2 hours
3. The PVC has not yet been accessed for treatment
4. Equal to or more than 18 years of age (no upper limit)
5. Able to provide written informed consent.
•Current blood stream infection (within 48 hours of study entry, with the exclusion of a single common skin contaminant as per NHSN)
•Non-English speaker without interpreter
•Previous enrolment in this study
•On a palliative care pathway and/or receiving critical care treatment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method