Skip to main content
Clinical Trials/NCT00915824
NCT00915824
Unknown
Phase 4

Prevention of Potentially Inappropriate Prescribing in Late Life Using STOPP (Screening Tool of Older Persons' Potentially Inappropriate Prescriptions) and START (Screening Tool to Alert Doctors to Right i.e. Appropriate Indicated Treatment): A Randomized Controlled Trial.

Cork University Hospital1 site in 1 country400 target enrollmentNovember 2007
ConditionsHealthy

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Healthy
Sponsor
Cork University Hospital
Enrollment
400
Locations
1
Primary Endpoint
Appropriateness of prescribing using the Medication Appropriateness Index and the Assessment of Underutilization of Medication Tool
Last Updated
16 years ago

Overview

Brief Summary

Potentially inappropriate prescribing is common in older patients and encompasses overuse, misuse and underuse of medications. Potentially inappropriate prescribing is associated with negative outcomes including adverse drug events and hospitalization.

STOPP (Screening Tool of Older Person's potentially inappropriate Prescriptions) and START (Screening Tool to Alert doctors to Right Treatment) is a new screening tool designed to detect instances of potentially inappropriate medication use and under-prescribing of clinically indicated medications in older patients. The purpose of this study is to determine whether clinical implementation of STOPP/START criteria in hospitalized older patients is effective in improving prescribing quality.

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
June 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All patients aged 65 years and older admitted to the general medical services of Cork University Hospital, Cork, Ireland

Exclusion Criteria

  • Patient admitted to a geriatric medicine service, psychiatry of old age service or clinical pharmacology service, or under review of these services during the previous 12 months
  • Critically ill patient (admitted to the intensive care unit)
  • Terminally ill patient
  • Refusal of patient or hospital physician to participate
  • No time for the research physician to enrol the patient within 3 days of admission

Outcomes

Primary Outcomes

Appropriateness of prescribing using the Medication Appropriateness Index and the Assessment of Underutilization of Medication Tool

Time Frame: Measured on admission, discharge and at 2, 4 and 6 months post-discharge

Secondary Outcomes

  • Composite health resource utilization including hospital readmission and primary care consultations(at 2, 4 and 6 months post-discharge)

Study Sites (1)

Loading locations...

Similar Trials