Clinical Trials Directory

Trials / Completed

CompletedNCT02474810

Intensive Versus Standard Hemodialysis CVC Dysfunction Protocol

Comparison of an Intensive Versus a Standard Hemodialysis Central Venous Catheter Dysfunction Protocol Using Alteplase

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Nova Scotia Health Authority · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Central venous catheters (CVCs) are used for vascular access by approximately 56% of our 380 hemodialysis (HD) patients at the Capital Health Renal Program. The major complication of these catheters includes thrombosis and infection. Catheter locking solutions such as recombinant tissue plasminogen activator (rt-PA), Alteplase (Cathflo®) are used to treat and prevent clotting of the catheter during HD treatments and during the interdialytic period. Evidence to guide the use of rt-PA is limited. This quality assurance project will compare the effectiveness and cost of an intensive versus a standard catheter dysfunction protocol for rt-PA in HD patients.

Detailed description

The proposed study will be a retrospective cohort study of consecutive HD patients conducted at a HD unit using two catheter dysfunction protocols during January 2013 to Septebmer 2013. In the Intensive Protocol, rt-PA intervention is administered to all catheters based on blood flow and/or line reversal. In the Standard Protocol, rt-PA intervention is administered to all catheters based only on blood flow.

Conditions

Interventions

TypeNameDescription
DRUGAlteplaseAlteplase for CVC dysfunction.

Timeline

Start date
2013-01-01
Primary completion
2015-07-01
Completion
2015-09-01
First posted
2015-06-18
Last updated
2024-08-21

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02474810. Inclusion in this directory is not an endorsement.