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Intravascular device administration sets: Replacement after Standard Versus Prolonged use (The RSVP Trial)

Intravascular device (IVD) administration sets: a comparison of IVD-related Bloodstream Infection between Replacement after Standard Versus Prolonged use (The RSVP Trial)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000505000
Acronym
RSVP
Enrollment
2941
Registered
2010-06-18
Start date
2011-05-30
Completion date
2016-12-09
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

IVD insertion is the most common invasive healthcare procedure with approximately 14 million IVDs used in Australia each year. IVDs alone are inadequate to deliver most therapy and require connection to an administration set. These IVD administration sets (AS) refer to infusion systems comprised of some or all of: tubing, fluid containers, pressure monitoring transducers, blood sampling ports, measuring burettes and extension tubing. IVDs and their AS break the natural defence barrier of the skin, and are the single most important cause of healthcare acquired blood stream infection (BSI). Most IVD's are replaced every 3 -4 days , however preliminary research suggests routine replacement of AS every 4 days costs Australia about $1 billion annually, and some studies suggest 7 day use would reduce costs with no threat to patient safety.

Interventions

Patients in this study have intravascular devices (IVDs) used in medical, surgical, intensive care, oncology and haematology units, and include adult and paediatric patients. Patients will have their administration set replaced every 7 days. This will continue for the course of their intravenous (IV) therapy.

Sponsors

Griffith University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No

Inclusion criteria

1. Informed written consent or waived consent (as per approving HREC) 2. Central venous or peripheral arterial IVD in situ. 3. IVD and AS have been insitu for equal to or more than 24 hours 4. IVD scheduled/expected use equal to or more than 7 days

Exclusion criteria

Current bloodstream infection (within the previous 48 hours) Planned removal of device less than or equal to 24 hours IVD in situ >96 hours Original AS already routinely replaced

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 23, 2026