High-Flow Needleless Valve and DualCap Disinfection Devices Associate With Catheter-related Bloodstream Infection
Phase 4
- Conditions
- Catheter-related Bloodstream Infection
- Interventions
- Device: High-Flow Needleless ValveDevice: DualCap Disinfection Devices
- Registration Number
- NCT02990923
- Lead Sponsor
- Peking University First Hospital
- Brief Summary
The purpose of this study is to investigate whether the usage of High-Flow Needleless Valve and DualCap Disinfection Devices would reduce the incidence of catheter-related bloodstream infection in hemodialysis patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 102
Inclusion Criteria
- Implanted non-tunneled cuff catheter for any reason and going on blood purified therapy in our centre
- Have signed information consent form
Exclusion Criteria
- Have got bacteremia before catheter implantation
- Catheter changing in situ
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Only High-Flow Valve High-Flow Needleless Valve In this group, patients will use High-Flow Needleless Valve instead of traditional standard hemodialysia connector, but still receiving typical disinfection management Both Divices High-Flow Needleless Valve In this group, patients will receive both High-Flow Needleless Valve and DualCap Disinfection Devices in hemodialysis Both Divices DualCap Disinfection Devices In this group, patients will receive both High-Flow Needleless Valve and DualCap Disinfection Devices in hemodialysis
- Primary Outcome Measures
Name Time Method Catheter-related bloodstream infection through study completion, an average of 1 year
- Secondary Outcome Measures
Name Time Method Number of participants with catheter withdraw for any reason through study completion, an average of 1 year Number of participants with catheter dysfunction through study completion, an average of 1 year