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Clinical Trial Summary

The purpose of this study is to determine the benefit of patients using a multidrug blister packs after discharged from an university hospital to their homes.


Clinical Trial Description

Typical adherence rates for oral prescription medications are approximately 50-76%. Insufficient adherence causes an increase in morbidity, mortality, and costs, and decreases quality of life of patients. Multidrug blister packs are recommended to improve adherence and are widely used in Switzerland. However, evidence is poor and patient-relevant endpoints are seldom measured. This study was designed to compare patient-relevant outcomes in patients with medication repackaged in multidrug blister packs versus patients with medication dispensed in commercially available packages. Adherence of the intervention group will be monitored electronically and feedback will be given to the patients. The intervention will take place in a study pharmacy. Follow-up visits will take place at the study pharmacy at 3, 6, and 12 months for all patients. Study duration will be 12 months. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms

  • Any Event Leading to Hospitalisation
  • Blister

NCT number NCT01759095
Study type Interventional
Source University Hospital, Basel, Switzerland
Contact
Status Terminated
Phase N/A
Start date January 2013
Completion date December 2014