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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

Tracking Information
First Submitted Date May 11, 2010
First Posted Date May 13, 2010
Last Update Posted Date July 8, 2011
Study Start Date May 2010
Actual Primary Completion Date May 2011   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Rational Fluid Therapy in Germany
Official Title Klinisches Register RaFTinG - Rational Fluid Therapy in Germany
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.
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.

Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population Patients in intensive care units with an indication for fluid/volume therapy
Condition Patients in ICU
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Ertmer C, Zwißler B, Van Aken H, Christ M, Spöhr F, Schneider A, Deisz R, Jacob M. Fluid therapy and outcome: a prospective observational study in 65 German intensive care units between 2010 and 2011. Ann Intensive Care. 2018 Feb 17;8(1):27. doi: 10.1186/s13613-018-0364-z.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Unknown status
Estimated Enrollment
 (submitted: July 7, 2011)
4000
Original Estimated Enrollment
 (submitted: May 12, 2010)
3000
Estimated Study Completion Date October 2011
Actual Primary Completion Date May 2011   (Final data collection date for primary outcome measure)
Eligibility 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
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Germany
Removed Location Countries  
 
Administrative Information
NCT Number NCT01122277
Other Study ID Numbers 337 -09/2009-366-f-S
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party PD Dr. Matthias Jacob, Klinikum der Universität München, Klinik für Anaesthesiologie
Study Sponsor Ludwig-Maximilians - University of Munich
Collaborators
  • University Hospital Muenster
  • Fresenius Kabi, Bad Homburg, Germany
Investigators
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
PRS Account Ludwig-Maximilians - University of Munich
Verification Date October 2010