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Controlling device Occlusion by needleless ConnectOr design. A pilot randomised control trial (COCOA Trial)

Not Applicable
Completed
Conditions
Peripheral intravenous catheter failure
Public 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
Inclusion Criteria

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.

Exclusion Criteria

•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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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