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High-Flow Needleless Valve and DualCap Disinfection Devices Associate With Catheter-related Bloodstream Infection

P

Peking University

Status and phase

Unknown
Phase 4

Conditions

Catheter-related Bloodstream Infection

Treatments

Device: DualCap Disinfection Devices
Device: High-Flow Needleless Valve

Study type

Interventional

Funder types

Other

Identifiers

NCT02990923
PekingHDNC

Details and patient eligibility

About

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.

Enrollment

102 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 3 patient groups

Control
No Intervention group
Description:
In this group, patients will use traditional standard hemodialysis connector and receive typical disinfection management
Only High-Flow Valve
Experimental group
Description:
In this group, patients will use High-Flow Needleless Valve instead of traditional standard hemodialysia connector, but still receiving typical disinfection management
Treatment:
Device: High-Flow Needleless Valve
Both Divices
Experimental group
Description:
In this group, patients will receive both High-Flow Needleless Valve and DualCap Disinfection Devices in hemodialysis
Treatment:
Device: DualCap Disinfection Devices
Device: High-Flow Needleless Valve

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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