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Barriers to the Implementation of Complete Insulin Order Sets

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00813280
First Posted: December 23, 2008
Last Update Posted: November 26, 2015
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.
Collaborators:
International Diabetes Center at Park Nicollet
Park Nicollet Foundation
Information provided by:
HealthPartners Institute
  Purpose
The major purpose of this Quality Improvement project is to begin to address the issues surrounding glycemic control in the hospital setting by collecting accurate, reliable and verifiable data on the occurrence of hyperglycemia (BG >300 mg/dL), and whether or not CIO is used (immediately before and 72 hours after the BG >300 mg/dl).

Condition
Hyperglycemia

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Barriers to the Implementation of Complete Insulin Order Sets in the Management of Individuals With Hyperglycemia or Diabetes at Park Nicollet Methodist Hospital

Resource links provided by NLM:


Further study details as provided by HealthPartners Institute:

Primary Outcome Measures:
  • glucose levels [ Time Frame: 72 hours ]

Secondary Outcome Measures:
  • type of insulin treatment [ Time Frame: 72 hours ]

Enrollment: 200
Study Start Date: June 2008
Study Completion Date: December 2008
Primary Completion Date: September 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts
hyperglycemia
hospitalized patients with BG >300 ml/dL

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
hospitalized patients with blood glucose >300 mg/dL
Criteria

Inclusion Criteria:

  • Park Nicollet Methodist Hospital patient
  • recorded BG > 300 mg/dL during the study data collection period
  • admitted to general floor hospital units

Exclusion Criteria:

  • birth center
  • intensive care units
  • eating disorder unit
  • pediatric patients < 18 years of age
  • patients receiving insulin infusions
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00813280


Locations
United States, Minnesota
Park Nicollet Methodist Hospital
Minneapolis, Minnesota, United States, 55416
Sponsors and Collaborators
HealthPartners Institute
International Diabetes Center at Park Nicollet
Park Nicollet Foundation
Investigators
Principal Investigator: Lisa Fish, MD Park Nicollet Health Services Endocrinology
Principal Investigator: Robert M Cuddihy, MD International Diabetes Center at Park Nicollet
  More Information
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