Comparison of Two New Generations Dressings in Intensive Care Unit
NCT ID: NCT01795391
Last Updated: 2014-01-22
Study Results
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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COMPLETED
685 participants
OBSERVATIONAL
2012-10-31
2013-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Tegaderm HP
Patients whose intravasculare devices dressings are made exclusevely with Tegaderm HP dressings.
No interventions assigned to this group
Advanced
Patients whose intravasculare devices dressings are made exclusevely with Advanced dressings
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients benefiting from the social security protection.
Exclusion Criteria
* Patients having known allergy or sensitivity to adhesive dressing materials
18 Years
ALL
No
Sponsors
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University Hospital, Grenoble
OTHER
Responsible Party
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Locations
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University Hospital of Grenoble, Medical Intensive Care Unit
Grenoble, Isère, France
Countries
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Other Identifiers
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ADVANCED
Identifier Type: -
Identifier Source: org_study_id
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