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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01122277
Other study ID # 337 -09/2009-366-f-S
Secondary ID
Status Active, not recruiting
Phase N/A
First received May 11, 2010
Last updated July 7, 2011
Start date May 2010
Est. completion date October 2011

Study information

Verified date October 2010
Source Ludwig-Maximilians - University of Munich
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 4000
Est. completion date October 2011
Est. primary completion date May 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Klinik für Anaesthesiologie, Klinikum der Universität München Munich Bavaria
Germany Universitätsklinikum Münster Münster Nordrhein - Westfalen

Sponsors (3)

Lead Sponsor Collaborator
Ludwig-Maximilians - University of Munich Fresenius Kabi, Bad Homburg, Germany, University Hospital Muenster

Country where clinical trial is conducted

Germany, 

See also
  Status Clinical Trial Phase
Not yet recruiting NCT03195439 - Temple Touch Pro (TTP) Non-Invasive Core Temperature Monitoring as a Measure for Early Detection of Fever Related Infections, Including Sepsis. N/A