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Influence of Perioperative Kidney Function on Postoperative Outcome (NEPHRANEST)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01522313
First Posted: January 31, 2012
Last Update Posted: October 10, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Claudia Spies, Charite University, Berlin, Germany
January 23, 2012
January 31, 2012
October 10, 2012
January 2006
June 2012   (Final data collection date for primary outcome measure)
hospital length of stay [ Time Frame: 1 year ]
once per case
Same as current
Complete list of historical versions of study NCT01522313 on ClinicalTrials.gov Archive Site
all cause in-hospital mortality [ Time Frame: 1 year ]
occurrence during hospital stay
Same as current
Not Provided
Not Provided
 
Influence of Perioperative Kidney Function on Postoperative Outcome
Retrospective Data Analysis of the Impact of Perioperative Kidney Function on Postoperative Outcome
This study investigates the influence of perioperative changes in serum creatinine on hospital length of stay and mortality.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Retrospective
Not Provided
Not Provided
Non-Probability Sample
Retrsospective analysis of electronic charts of all patients that underwent anesthesia between January 2006 - June 2012 in the Department of Anesthesiology at the Charité - University Medicine Berlin, Campus Charité Mitte und Campus Virchow Klinikum.
  • Renal Insufficiency
  • Acute Kidney Injury
Not Provided
Patients
Data of patients anesthetized in the years 2006 to 2012 (Hospital stay: January 2006 - June 2012) will be analysed in the study.
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
39369
June 2012
June 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • all patients anesthetized between January 2006 - June 2012

Exclusion Criteria:

  • end stage renal disease
  • pre-anesthesiologic need of renal replacement therapy
  • patients undergoing nephrectomy or kidney transplantation
Sexes Eligible for Study: All
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
 
NCT01522313
NEPHRANEST
No
Not Provided
Not Provided
Claudia Spies, Charite University, Berlin, Germany
Charite University, Berlin, Germany
Not Provided
Principal Investigator: Claudia D Spies, MD Prof. Charite University, Berlin, Germany
Charite University, Berlin, Germany
October 2012