Product Evaluation for the Effectiveness of the ClearGuard® HD End Cap
Completed · Not applicable
Conditions studied: End Stage Renal Disease (ESRD)
In brief
To assess blood stream infections in participants using two FDA-cleared devices: ClearGuard HD end caps compared to the Tego® connector with the CurosTM for Tego disinfecting port protector.
Key facts
- Study ID
- NCT02593149
- Run by
- Pursuit Vascular, Inc.
- People needed
- 1902
- Starts
- 2015-11-01
- Expected to finish
- 2016-11-01
- Last updated by the study team
- 2019-02-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients dialyzing with a central venous catheter
You may not qualify if…
- Known allergy to chlorhexidine
Where it is running
- DaVita Clinical Research — Minneapolis, Minnesota, United States
Full record on ClinicalTrials.gov
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