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Clinical Trials/ISRCTN45894687
ISRCTN45894687
Completed
N/A

An educational intervention to improve adverse drug reactions reporting: a cluster-randomised trial among Portuguese physicians and pharmacists

Educational Development Program for Portugal (Programa de Desenvolvimento Educativo para Portugal) (PRODEP) (Portugal)0 sites1,433 target enrollmentJune 15, 2006

Overview

Phase
N/A
Intervention
Not specified
Conditions
nder-reporting of adverse drug reactions
Sponsor
Educational Development Program for Portugal (Programa de Desenvolvimento Educativo para Portugal) (PRODEP) (Portugal)
Enrollment
1433
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

2008 results in: https://www.ncbi.nlm.nih.gov/pubmed/18366244 (added 11/07/2019)

Registry
who.int
Start Date
June 15, 2006
End Date
June 30, 2005
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Educational Development Program for Portugal (Programa de Desenvolvimento Educativo para Portugal) (PRODEP) (Portugal)

Eligibility Criteria

Inclusion Criteria

  • All National Health System physicians working in the Northern Region of Portugal and all pharmacists working in the same geographical area.

Exclusion Criteria

  • Physicians not involved in any clinical activity (e.g. engaged in administrative tasks, analysis, etc.); working in substance abuse and rehabilitation centers; working at the regional pharmacosurveillance center or any department having a specific voluntary adverse drug reaction reporting program and physicians attached to specific hospitals (cancer, maternity, etc). Pharmacists working at the regional pharmacosurveillance center and attached to specific hospitals (cancer, maternity, etc).

Outcomes

Primary Outcomes

Not specified

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