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Trial record 1 of 1 for:    NCT01122277
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Rational Fluid Therapy in Germany (RaFTinG)

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ClinicalTrials.gov Identifier: NCT01122277
Recruitment Status : Unknown
Verified October 2010 by Ludwig-Maximilians - University of Munich.
Recruitment status was:  Active, not recruiting
First Posted : May 13, 2010
Last Update Posted : July 8, 2011
Sponsor:
Collaborators:
University Hospital Muenster
Fresenius Kabi, Bad Homburg, Germany
Information provided by:
Ludwig-Maximilians - University of Munich

Brief Summary:
The purpose of this observational study is the prospective documentation and evaluation of the status quo of volume therapy in German intensive care units.

Condition or disease
Patients in ICU

Detailed Description:

The purpose of RaFTinG is the prospective documentation and evaluation of the demographic, diagnostic and therapeutic characteristics of unselected patients and their treatment in intensive care units (ICU) in Germany.

Documentation will not only include their stay in the ICU but a follow up query 90 days after discharge from the ICU.

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Study Type : Observational
Estimated Enrollment : 4000 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Klinisches Register RaFTinG - Rational Fluid Therapy in Germany
Study Start Date : May 2010
Actual Primary Completion Date : May 2011
Estimated Study Completion Date : October 2011




Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients in intensive care units with an indication for fluid/volume therapy
Criteria

Inclusion Criteria:

  • ICU patients with an indication for fluid/volume therapy

Exclusion Criteria:

  • Patients hospitalized by order of a court of law or a government agency

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01122277


Locations
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Germany
Klinik für Anaesthesiologie, Klinikum der Universität München
Munich, Bavaria, Germany, 80336
Universitätsklinikum Münster
Münster, Nordrhein - Westfalen, Germany, 48149
Sponsors and Collaborators
Ludwig-Maximilians - University of Munich
University Hospital Muenster
Fresenius Kabi, Bad Homburg, Germany
Investigators
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Principal Investigator: Matthias Jacob, MD Klinik für Anaesthesiologie, Klinikum der Universität München
Principal Investigator: Christian Ertmer, MD Universitätsklinikum Münster, Germany
Study Chair: Bernhard Zwissler, Prof Klinik für Anaesthesiologie, Klinikum der Universität München, Germany
Study Chair: Hugo van Aken, Prof Universitätsklinikum Münster, Germany
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: PD Dr. Matthias Jacob, Klinikum der Universität München, Klinik für Anaesthesiologie
ClinicalTrials.gov Identifier: NCT01122277    
Other Study ID Numbers: 337 -09/2009-366-f-S
First Posted: May 13, 2010    Key Record Dates
Last Update Posted: July 8, 2011
Last Verified: October 2010
Keywords provided by Ludwig-Maximilians - University of Munich:
Volume therapy
Fluid therapy
Patients in ICU