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

NCT ID: NCT02990923

Last Updated: 2016-12-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

102 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Brief Summary

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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

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Conditions

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Catheter-related Bloodstream Infection

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Control

In this group, patients will use traditional standard hemodialysis connector and receive typical disinfection management

Group Type NO_INTERVENTION

No interventions assigned to this group

Only High-Flow Valve

In this group, patients will use High-Flow Needleless Valve instead of traditional standard hemodialysia connector, but still receiving typical disinfection management

Group Type EXPERIMENTAL

High-Flow Needleless Valve

Intervention Type DEVICE

Both Divices

In this group, patients will receive both High-Flow Needleless Valve and DualCap Disinfection Devices in hemodialysis

Group Type EXPERIMENTAL

High-Flow Needleless Valve

Intervention Type DEVICE

DualCap Disinfection Devices

Intervention Type DEVICE

Interventions

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High-Flow Needleless Valve

Intervention Type DEVICE

DualCap Disinfection Devices

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking University First Hospital

OTHER

Sponsor Role lead

Responsible Party

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Rong Xu

vice professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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PekingHDNC

Identifier Type: -

Identifier Source: org_study_id