Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Influence of Perioperative Kidney Function on Postoperative Outcome (NEPHRANEST)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Claudia Spies, Charite University, Berlin, Germany
ClinicalTrials.gov Identifier:
NCT01522313
First received: January 23, 2012
Last updated: October 8, 2012
Last verified: October 2012

January 23, 2012
October 8, 2012
January 2006
June 2012   (final data collection date for primary outcome measure)
hospital length of stay [ Time Frame: 1 year ] [ Designated as safety issue: No ]
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 ] [ Designated as safety issue: No ]
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
Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT01522313
NEPHRANEST
No
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

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP