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Medication Reconciliation in Comparison to an Extensive Medication Safety Check

Pilot Project to Investigate the Influence of Medication Reconciliation and an Extensive Medication Safety Check on the Number of Adverse Drug Events in the Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02413957
Enrollment
220
Registered
2015-04-10
Start date
2015-01-31
Completion date
2016-01-31
Last updated
2017-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adverse Drug Event, Elderly

Keywords

Elderly Patients, Medication Safety, Pharmaceutical Care, Medication Reconciliation

Brief summary

The purpose of this study is to determine wether an extensive medication safety check has a greater impact on the incidence of adverse drug events than medication reconciliation or no intervention.

Interventions

OTHERMedication Reconciliation

Pharmacist take the best possible medication history (BPMH), comparison of the BPMH with the admission order (AMO), clarify and solve al discrepancies between the BPMH and the AMO.

OTHERPharmaceutical Care

Checking medication under safety considerations (medication at admission, during hospital stay, at discharge); recommendations for inappropriate medication (e.g. contraindications or interactions) or medication related problems. Pharmaceutical care includes Medication Reconciliation.

Sponsors

Ärztliche Zentrum für Qualität in der Medizin
CollaboratorOTHER
Universitätsklinikum Bonn - Institut für Patientensicherheit
CollaboratorUNKNOWN
RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient 65 years and older * written informed consent patient or the legal representative * existing medication therapy at hospitalization * admission to one of the project wards via emergency department (non elective)

Exclusion criteria

\- patients included in the study previously

Design outcomes

Primary

MeasureTime frame
incidence of adverse drug events1 year

Secondary

MeasureTime frameDescription
Assessment of the clinical relevance of medication related problems as determined by the French Society of Clinical Pharmacy1 yearSeverity scale for medication related problems: minor, significative, major, critical, catastrophic
Assessment of the clinical relevance of discrepancies as determined by the French Society of Clinical Pharmacy1 yearSeverity scale for discrepancies: minor, significative, major, critical, catastrophic
number of medication related problems1 year
number of discrepancies1 year
duration of taking the best possible medication history1 yearThe duration is measured in minutes.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026