NCT01522313

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
39,369

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2006

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2006

Completed
6.1 years until next milestone

First Submitted

Initial submission to the registry

January 23, 2012

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 31, 2012

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2012

Completed
Last Updated

October 10, 2012

Status Verified

October 1, 2012

Enrollment Period

6.4 years

First QC Date

January 23, 2012

Last Update Submit

October 8, 2012

Conditions

Renal InsufficiencyAcute Kidney Injury

Outcome Measures

Primary Outcomes (1)

  • hospital length of stay

    once per case

    1 year

Secondary Outcomes (1)

  • all cause in-hospital mortality

    1 year

Study Arms (1)

Patients

Data of patients anesthetized in the years 2006 to 2012 (Hospital stay: January 2006 - June 2012) will be analysed in the study.

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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.

You may qualify if:

  • all patients anesthetized between January 2006 - June 2012

You may not qualify if:

  • end stage renal disease
  • pre-anesthesiologic need of renal replacement therapy
  • patients undergoing nephrectomy or kidney transplantation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Charité - University Medicine Berlin

Berlin, 13353, Germany

Location

MeSH Terms

Conditions

Renal InsufficiencyAcute Kidney Injury

Condition Hierarchy (Ancestors)

Kidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital Diseases

Study Officials

  • Claudia D Spies, MD Prof.

    Charite University, Berlin, Germany

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Anesthesiology

Study Record Dates

First Submitted

January 23, 2012

First Posted

January 31, 2012

Study Start

January 1, 2006

Primary Completion

June 1, 2012

Study Completion

June 1, 2012

Last Updated

October 10, 2012

Record last verified: 2012-10

Locations

DE(1)