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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00569322
Other study ID # 01817-03-C
Secondary ID
Status Completed
Phase N/A
First received December 5, 2007
Last updated November 25, 2015
Start date December 2003
Est. completion date September 2004

Study information

Verified date September 2007
Source HealthPartners Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Determine if routine BG testing at the time of ICU admission is being done on all patients, irrespective of a prior diagnosis of diabetes mellitus, and whether it provides clinically important information.


Description:

This prospective, observational study was performed in the medical-surgical ICU of a single hospital within a large multi-specialty healthcare system.

It was determined that it was not standard care to do glucose testing on all patients admitted to medical/surgical ICU's who did not have diagnosed diabetes and varied widely with the admitting service.

The primary objective of the study was to assess the availability and clinical value of blood glucose testing at the time of ICU admission after testing was implemented as routine care in the ICU.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date September 2004
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ICU Admission

Exclusion Criteria:

- < 18 years of age

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
BG Test


Locations

Country Name City State
United States Methodist Hospital - Park Nicollet Health Services Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
HealthPartners Institute

Country where clinical trial is conducted

United States, 

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