Clinical Trials Directory

Trials / Completed

CompletedNCT01243710

Taurolidine in Haemodialysis Catheter Related Bacteraemia

A Randomised Controlled Trial of Taurolidine With Heparin for Prevention of Recurrence of Catheter Related Bacteraemia in Haemodialysis Patients.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
27 (actual)
Sponsor
Imperial College Healthcare NHS Trust · Academic / Other
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether taurolidine with heparin locking solution prevents recurrence of central venous catheter related blood stream infections in haemodialysis patients.

Detailed description

Infections related to long-term haemodialysis catheters are associated with significant morbidity. A high proportion of those people initially treated with antibiotics to clear a catheter infection develop a second infection within six months, necessitating the removal and replacement of the dialysis catheter. This study will examine the efficacy of an antimicrobial catheter locking solution called taurolidine with heparin in preventing a second infection within six months of a significant infection. This solution will be compared with the solution used currently (heparin) which is left inside the catheter between dialysis sessions. This is a clinical study given that antimicrobial catheter locks are thought to reduce the risk of blood stream infections and the ultimate need for catheter change. However, there is concern that the absence of an anticoagulant in the lock solution increases the risk of catheter thrombosis, again requiring a change of catheter but for a separate reason. It is unclear therefore whether a solution containing both taurolidine (an antimicrobial) and heparin (an anticoagulant) will increase catheter survival. The results of this study will help guide the appropriate suse of locking solutions in the future.

Conditions

Interventions

TypeNameDescription
DEVICETaurolidine with heparin (500 units/ ml)Central venous catheter will be locked (the designated volume required to fill the dead space) with taurolidine with heparin after each dialysis session. The control arm will be locked with heparin as is current practice.

Timeline

Start date
2010-08-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2010-11-18
Last updated
2020-07-30

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT01243710. Inclusion in this directory is not an endorsement.