Influence of Perioperative Kidney Function on Postoperative Outcome

Acute Kidney Injury Clinical Trial

— NEPHRANEST  

Official title:

Retrospective Data Analysis of the Impact of Perioperative Kidney Function on Postoperative Outcome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01522313
• Other study ID #: NEPHRANEST
• Status: Completed
• Phase: N/A
• First received: January 23, 2012
• Last updated: October 8, 2012
• Start date: January 2006
• Est. completion date: June 2012

Study information

• Verified date: October 2012
• Source: Charite University, Berlin, Germany
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Ethics Commission
• Study type: Observational

Clinical Trial Summary

This study investigates the influence of perioperative changes in serum creatinine on hospital length of stay and mortality.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 39369
• Est. completion date: June 2012
• Est. primary completion date: June 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

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

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Acute Kidney Injury
• Renal Insufficiency

Locations

Country	Name	City	State
Germany	Charité - University Medicine Berlin	Berlin

Sponsors (1)

Lead Sponsor	Collaborator
Charite University, Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	hospital length of stay	once per case	1 year	No
Secondary	all cause in-hospital mortality	occurrence during hospital stay	1 year	No