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Improving Adherence to Prescribing Guidelines for Cholesterol Lowering in Hospitalized Diabetic Patients

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ClinicalTrials.gov Identifier: NCT01113099
Recruitment Status : Completed
First Posted : April 29, 2010
Last Update Posted : April 29, 2010
Sponsor:
Collaborator:
National Heart, Lung, and Blood Institute (NHLBI)
Information provided by:
Washington University School of Medicine

Brief Summary:
We hypothesize that when compared to usual care a greater proportion of hospitalized diabetic patients who are candidates for cholesterol lowering will be discharged with a prescription for a statin if their physicians are contacted by a pharmacist to discuss treatment guidelines.

Condition or disease Intervention/treatment Phase
Diabetes Dyslipidemia Other: Academic detailing Not Applicable

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 247 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Assisted Detailing to Improve Guideline Adherence
Study Start Date : June 2006
Actual Primary Completion Date : June 2007
Actual Study Completion Date : June 2007

Arm Intervention/treatment
Experimental: Academic detailing of physicians Other: Academic detailing
Education of physicians by pharmacists regarding indications for statins in diabetic patients

No Intervention: Usual care



Primary Outcome Measures :
  1. Statin prescription at hospital discharge [ Time Frame: Hospital discharge (avg = 3 days) ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Hospitalized patients with diabetes
  • LDL >= 100

Exclusion Criteria:

  • Terminal illness
  • Pregnancy
  • Intolerance or contraindication to statin

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): NCT01113099


Locations
United States, Missouri
Barnes Jewish Hospital
St. Louis, Missouri, United States, 63110
Sponsors and Collaborators
Washington University School of Medicine
National Heart, Lung, and Blood Institute (NHLBI)
Investigators
Principal Investigator: Thomas C Bailey, MD Washington University School of Medicine