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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00915824
Other study ID # CRT2006029
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received June 4, 2009
Last updated October 28, 2009
Start date November 2007
Est. completion date June 2009

Study information

Verified date October 2009
Source Cork University Hospital
Contact n/a
Is FDA regulated No
Health authority Ireland: Ministry of Health
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 400
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years and older
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
STOPP/START criteria
Application of STOPP/START criteria to the patient's prescription and diagnostic information with subsequent written recommendation on pharmaceutical care to the patient's medical team

Locations

Country Name City State
Ireland Cork University Hospital Cork

Sponsors (1)

Lead Sponsor Collaborator
Cork University Hospital

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Appropriateness of prescribing using the Medication Appropriateness Index and the Assessment of Underutilization of Medication Tool Measured on admission, discharge and at 2, 4 and 6 months post-discharge Yes
Secondary Composite health resource utilization including hospital readmission and primary care consultations at 2, 4 and 6 months post-discharge No
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