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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control | No Intervention | In this group, patients will use traditional standard hemodialysis connector and receive typical disinfection management | |
| Only High-Flow Valve | Experimental | In this group, patients will use High-Flow Needleless Valve instead of traditional standard hemodialysia connector, but still receiving typical disinfection management |
|
| Both Divices | Experimental | In this group, patients will receive both High-Flow Needleless Valve and DualCap Disinfection Devices in hemodialysis |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| High-Flow Needleless Valve | Device |
| ||
| DualCap Disinfection Devices |
| Measure | Description | Time Frame |
|---|---|---|
| Catheter-related bloodstream infection | through study completion, an average of 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Device |
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