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Flushing in Peripheral intravenous catheters (FliP): A pilot, randomised controlled trial of high versus low frequencies and volumes in patients with a peripheral venous catheter.

To assess the effectiveness of high frequency flushing versus low flushing frequency and volume on device failure in patients with a peripheral venous catheter: The FliP pilot trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000025538
Acronym
FliP
Enrollment
160
Registered
2015-01-19
Start date
2014-04-28
Completion date
2014-08-28
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

Venous cannulation via peripheral intravenous catheters (PIVC) is the simplest and most frequently used method for drug, fluid and blood product administration. Researchers estimate that up to 70% of patients in acute care hospitals require a PIVC. However, PIVC are associated with inherent complications which can be mechanical or infectious. Failure rates of these devices is unacceptably high, affecting up to 40% of patients receiving this therapy. Of these, 30% failed due to occlusion and infiltration (fluids into surrounding tissues) meaning patients had to have the PIVC replaced, which has implications for patient comfort, therapy and health care costs.There have been a range of strategies developed to prevent or reduce PIVC related complications including flushing regimes to maintain PIVC patency. However, current flushing practice is widely varied, with poor outcomes. There is little evidence that flushing of PIVC is actually happening in practice. To achieve best and evidence based practice it imperative that trial research is conducted to establish the best regime for maintaining PIVC patency. The study aims to establish the feasibility of conducting a four arm, factorial, randomized trial evaluating the efficacy and cost effectiveness of different flushing frequencies and volumes.

Interventions

Participants will have their peripheral cannula (PIVC) flushed with one of the following, until the patient requires PIVC removal, by the nurse providing care for the patient: 1) Flushed every 6 hours with 3 ml Sodium Chloride 0.9% 2) Flushed every 24 hours with 10 ml Sodium Chloride 0.9% 3) Flushed every 24 hours with 3 ml Sodium Chloride 0.9% AND pre and post medication administration.

Sponsors

Griffith University
Lead SponsorUniversity

Study design

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

Eligibility

Sex/Gender
All
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients greater than or equal to 16 years of age PIVC to be inserted for clinical care Informed consent to participate

Exclusion criteria

Planned removal of PIVC within next 24hrs Previous enrolment in the current study

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 12, 2026