Bundle Evaluation in Extra Renal Epuration, Incidence of Thrombosis
NCT ID: NCT01560364
Last Updated: 2014-12-02
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
100 participants
OBSERVATIONAL
2011-05-31
2012-08-31
Brief Summary
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Detailed Description
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The after phase will consist in medical measures (help for prescription) and paramedical measures (stop the filtration flow during the patient's mobilization).
Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Hemofilter
renal replacement therapy
Prospective observational clinical multicentric study in ICU with acute renal failure requiring renal replacement therapy.
Interventions
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renal replacement therapy
Prospective observational clinical multicentric study in ICU with acute renal failure requiring renal replacement therapy.
Eligibility Criteria
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Inclusion Criteria
* Renal replacement therapy (continuous veino-veinous hemofiltration or continuous veino-veinous hemodiafiltration)
* Consent of patients
Exclusion Criteria
* Age below 18 years
18 Years
ALL
No
Sponsors
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University Hospital, Clermont-Ferrand
OTHER
Responsible Party
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Principal Investigators
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Sébastien PERBET
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Clermont-Ferrand
Locations
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CHU Clermont-Ferrand
Clermont-Ferrand, , France
Countries
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Other Identifiers
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CHU-0106
Identifier Type: -
Identifier Source: org_study_id