Prevention of Adverse Drug Events (ADEs) in Hospitalised Older Patients

PHASE4CompletedINTERVENTIONAL
Enrollment

732

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

June 30, 2012

Study Completion Date

June 30, 2012

Conditions
Adverse Drug Reaction
Interventions
OTHER

Application of STOPP/START criteria

"The researcher will apply the STOPP/START criteria to the cases randomised to this intervention. This will occur at the point of recruitment into the study and consists of applying STOPP/START criteria to the list of prescribed medications the patient is taking at that time point.~Where potentially inappropriate medications (PIM's) are identified using the intervention, these are highlighted to the medical team with primary responsibility for the patient both verbally and in writing. The relevant registrar will be contacted in person or via telephone by the researcher and informed of the PIM's in addition to a standard medication advice form inserted into the patients' notes also highlighting the PIM's."

OTHER

Normal pharmaceutical care

The normal process of medication prescription and review by the attending medical team.

Trial Locations (1)

Unknown

Cork University Hospital, Cork

All Listed Sponsors
lead

University College Cork

OTHER

NCT01467050 - Prevention of Adverse Drug Events (ADEs) in Hospitalised Older Patients | Biotech Hunter | Biotech Hunter