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Clinical Trials/NCT00509717
NCT00509717
Completed
Not Applicable

Implementation of a Pharmacy-Intervention to Enhance Prescription and Use of Lipid-Lowering Drugs. A Randomized Trial.

Radboud University Medical Center1 site in 1 country70 target enrollmentOctober 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Diseases
Sponsor
Radboud University Medical Center
Enrollment
70
Locations
1
Primary Endpoint
The percentage of selected (=undertreated) patients receiving at least one prescription for lipid-lowering medication.
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to determine the effectiveness of maximal support of community pharmacies to implement a pharmaceutical care model for improving underprescription and treatment persistence regarding lipid-lowering medication in patients with cardiovascular disease.

Detailed Description

Cardiovascular disease is the main cause of death in large parts of the world. Next to life style changes, pharmaceutical treatment is a keystone in the treatment of cardiovascular disease. Despite the strong evidence for the effectiveness of lipid-lowering therapy, less than half of the people eligible are treated. With specific medication searches in the community pharmacy database, an easy tool for detecting patients who are undertreated is available. Based on this tool, a pharmaceutical care model for improving underprescription and treatment persistence regarding lipid-lowering medication in patients with cardiovascular disease was constructed. Moreover, it is not known yet how to implement this pharmaceutical care model in community pharmacies effectively. With multifaceted interventions the behaviour of health professionals can be changed. In this study the effectiveness of a maximal support strategy, including interactive educational meetings, reminders, audit and feedback, is compared to a minimal implementation strategy.

Registry
clinicaltrials.gov
Start Date
October 2006
End Date
March 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • pharmacies: resident in the south of the Netherlands
  • patients: with antiplatelet therapy and without lipid-lowering medication

Exclusion Criteria

  • for patients:
  • terminal disease
  • severe mental disorder

Outcomes

Primary Outcomes

The percentage of selected (=undertreated) patients receiving at least one prescription for lipid-lowering medication.

Time Frame: six months after the general practitioner received the list with selected patients

Secondary Outcomes

  • Differences in prescribing for age categories and co-medication.(six months)

Study Sites (1)

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