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Peripheral Venous Catheter Trial: 3 Day Versus No Routine Change - Article


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Day Care

Deafness




Clinical Trial: Peripheral Venous Catheter Trial: 3 Day Versus No Routine Change

This study is no longer recruiting patients.

Sponsored by: Royal Brisbane and Women's Hospital
Information provided by: Royal Brisbane and Women's Hospital

Purpose

The purpose of this study is to investigate the effects of extending the dwell time of peripheral intravenous cannulas on clinical outcomes and cost.

Condition Treatment or Intervention Phase
Phlebitis
 Procedure: Extending peripheral intravenous (IV) cannula dwell times
Phase II
Phase III

MedlinePlus related topics:  Thrombophlebitis

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study

Further Study Details: 
Primary Outcomes: Phlebitis during the course of the infusion and up to 48 hours after peripheral venous catheter removal
Secondary Outcomes: Infiltration permeation of IV fluid into the interstitial compartment; Local infection at the site of the catheter; Catheter-related blood stream infection; Catheter colonization; Cost
Expected Total Enrollment:  200

Study start: March 2004;  Study completion: December 2004
Last follow-up: December 2004;  Data entry closure: December 2004

Among hospitalized patients, intravenous therapy is the most common invasive procedure. It is associated with a phlebitis rate of between 1.1% and 63% and a central venous catheter related bacteremia rate of approximately 3.0%. Catheter related blood-stream infections have an attributable mortality rate of 12% to 25%. Factors thought to be associated with these complications include insertion techniques, catheter securement, type of catheter used, type of infusate and additives, post-insertion catheter care and length of time the catheter remains in place.

Current Centers of Disease Control Guidelines provide direction for intravenous therapy management including a recommendation that peripheral intravenous catheters should be re-sited every 72-96 hours. Data underpinning the recommendation was collected in 1992, over a decade ago. Since that time, there have been improvements in catheter design and composition, and prospective surveillance studies have demonstrated the safety of longer dwell times. To date, these observations have not been validated in adults, using randomized controlled trial methodology.

Re-siting intravenous cannulas causes discomfort to patients and has a high recurrent cost. The primary aim of the present study is to compare the rates of peripheral catheter-related blood stream infection, catheter-related local infection, phlebitis and obstruction between two groups of patients - those having routine catheter changes every 72 hours and those having catheter changes only when clinically indicated.

Specific hypotheses: That changing intravenous peripheral catheters when indicated by clinical signs compared to changing intravenous catheters every 3 days reduces the incidence of intravenous catheter related morbidity.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

Patients are eligible to join the Peripheral Venous Catheter Trial if:

  • They are inpatients at the Royal Brisbane and Royal Women's Hospital who are at least 18 years of age

AND

  • They are scheduled or expected to have a peripheral venous catheter indwelling for at least 4 days. AND
  • They have had their catheter inserted by a nurse from the IV Therapy Team

Exclusion Criteria:

  • Patients with an existing bloodstream infection
  • Those receiving immunosuppressive treatment

Location Information


Australia, Queensland
      Royal Brisbane and Women's Hospital, Brisbane,  Queensland,  4029,  Australia

More Information

Study ID Numbers:  RBWH 2003/131
Record last reviewed:  February 2005
Last Updated:  February 14, 2005
Record first received:  February 11, 2005
ClinicalTrials.gov Identifier:  NCT00103636
Health Authority: Australia: Department of Health and Ageing Therapeutic Goods Administration (Awaiting confirmation)
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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December 4, 2008



Page Updated: December 17, 2004
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