Urological and Genital Diseases: Haemodialysis Urological and Genital Diseases Haemodialysis
Conditions
Interventions
Patients will be recruited at the time of catheter insertion and randomised to one of two arms. Conventional practice (as defined by use of heparin locking with 5000 u/ml) and locking the catheter wit
Sponsors
Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Eligibility
Inclusion criteria
Inclusion criteria: Chronic haemodialysis patients
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| We will collect data on a variety of endpoints. Primary end point will be clinical infection rates. Data will also be collected on patency and thrombotic failure of catheters augmented with the data set relating to catheter function and dialysis adequacy that will be captured by the central server. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed