Improving Adherence to Prescribing Guidelines for Cholesterol Lowering in Hospitalized Diabetic Patients
This study has been completed.
Sponsor:
Washington University School of Medicine
Collaborator:
Information provided by:
Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT01113099
First received: April 22, 2010
Last updated: April 27, 2010
Last verified: April 2010
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Purpose
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 | Intervention |
|---|---|
|
Diabetes Dyslipidemia |
Other: Academic detailing |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Assisted Detailing to Improve Guideline Adherence |
Resource links provided by NLM:
Further study details as provided by Washington University School of Medicine:
Primary Outcome Measures:
- Statin prescription at hospital discharge [ Time Frame: Hospital discharge (avg = 3 days) ] [ Designated as safety issue: No ]
| Enrollment: | 247 |
| Study Start Date: | June 2006 |
| Study Completion Date: | June 2007 |
| Primary Completion Date: | June 2007 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Academic detailing of physicians |
Other: Academic detailing
Education of physicians by pharmacists regarding indications for statins in diabetic patients
|
| No Intervention: Usual care |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Hospitalized patients with diabetes
- LDL >= 100
Exclusion Criteria:
- Terminal illness
- Pregnancy
- Intolerance or contraindication to statin
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01113099
Locations
| United States, Missouri | |
| Barnes Jewish Hospital | |
| St. Louis, Missouri, United States, 63110 | |
Sponsors and Collaborators
Washington University School of Medicine
Investigators
| Principal Investigator: | Thomas C Bailey, MD | Washington University School of Medicine |
More Information
Publications:
| Responsible Party: | Thomas C Bailey/Professor of Medicine, Washington University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT01113099 History of Changes |
| Other Study ID Numbers: | 02-1072, R01HL070790 |
| Study First Received: | April 22, 2010 |
| Last Updated: | April 27, 2010 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases |
ClinicalTrials.gov processed this record on May 22, 2013