Bundle Evaluation in Extra Renal Epuration, Incidence of Thrombosis (BEERT)
This study is currently recruiting participants.
Verified March 2012 by University Hospital, Clermont-Ferrand
Sponsor:
University Hospital, Clermont-Ferrand
Information provided by (Responsible Party):
University Hospital, Clermont-Ferrand
ClinicalTrials.gov Identifier:
NCT01560364
First received: October 17, 2011
Last updated: March 20, 2012
Last verified: March 2012
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Purpose
Detailed Description:
This is a prospective observational clinical multicentric study in ICU with acute renal failure requiring renal replacement therapy.
Condition | Intervention |
---|---|
Adults Receiving Renal Replacement Therapy |
Other: renal replacement therapy |
Study Type: | Observational |
Study Design: | Time Perspective: Prospective |
Official Title: | Bundle Evaluation in Extra Renal Epuration, Incidence of Thrombosis |
Further study details as provided by University Hospital, Clermont-Ferrand:
Primary Outcome Measures:
- Hemofilter lifetime [ Time Frame: at day 1 ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
- Hemofilter clotting risk factors [ Time Frame: at day 1 ] [ Designated as safety issue: Yes ]
- hemofiltration duration [ Time Frame: at day 1 ] [ Designated as safety issue: Yes ]
- down time value [ Time Frame: at day 1 ] [ Designated as safety issue: Yes ]
Estimated Enrollment: | 100 |
Study Start Date: | May 2011 |
Estimated Study Completion Date: | November 2012 |
Estimated Primary Completion Date: | November 2012 (Final data collection date for primary outcome measure) |
Groups/Cohorts | Assigned Interventions |
---|---|
Hemofilter |
Other: renal replacement therapy
Prospective observational clinical multicentric study in ICU with acute renal failure requiring renal replacement therapy.
|
Detailed Description:
Prospective before / after observational clinical multicentric study on ICU acute kidney injury during renal replacement therapy. Evaluation of incidence and exposure to hemofilter clotting.
The after phase will consist in medical measures (help for prescription) and paramedical measures (stop the filtration flow during the patient's mobilization).
Eligibility
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Study Population
Adults receiving renal replacement therapy
Criteria
Inclusion Criteria:
- Adult (age > 18 years)
- Renal replacement therapy (continuous veino-veinous hemofiltration or continuous veino-veinous hemodiafiltration)
- Consent of patients
Exclusion Criteria:
- Use citrate anticoagulation
- Age below 18 years
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01560364
Contacts
Contact: Patrick LACARIN | 04 73 75 11 95 | placarin@chu-clermontferrand.fr |
Locations
France | |
CHU Clermont-Ferrand | Recruiting |
Clermont-Ferrand, France, 63003 | |
Contact: Patrick LACARIN 04 73 75 11 95 placarin@chu-clermontferrand.fr |
Sponsors and Collaborators
University Hospital, Clermont-Ferrand
Investigators
Principal Investigator: | Sébastien PERBET | University Hospital, Clermont-Ferrand |
More Information
No publications provided
Keywords provided by University Hospital, Clermont-Ferrand:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 17, 2012
No publications provided
Responsible Party: | University Hospital, Clermont-Ferrand |
ClinicalTrials.gov Identifier: | NCT01560364 History of Changes |
Other Study ID Numbers: | CHU-0106 |
Study First Received: | October 17, 2011 |
Last Updated: | March 20, 2012 |
Health Authority: | France: Ministry of Health |
Keywords provided by University Hospital, Clermont-Ferrand:
Renal replacement therapy Hemofilter clotting Clotting risk factor Hemofilter clotting prevention |
Additional relevant MeSH terms:
Thrombosis Embolism and Thrombosis Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on October 17, 2012