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Medication Safety of Elderly Patients in Hospital and Ambulatory Setting

Medication Safety of Elderly Patients in Hospital and Ambulatory Setting Considering the Transitions of Care for Home-cared Patients and Nursing Home Residents

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01578525
Enrollment
61
Registered
2012-04-17
Start date
2012-04-30
Completion date
2014-04-30
Last updated
2015-10-30

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

Conditions

Elderly, Health Services for the Aged, Hospital Readmission, Medication Safety, Pharmaceutical Care

Keywords

medication safety, elderly, pharmaceutical care, hospital readmission, drug-related readmission, Health Services for the Aged

Brief summary

The purpose of this study is to determine whether additional pharmaceutical care for elderly patients (home-cared patients, nursing-home residents) has a positive impact on drug-related readmissions.

Interventions

Checking medication under safety considerations (medication at admission, hospitalization, discharge); recommendations for potentially inappropriate medication (PRISCUS-criteria),

Sponsors

Apothekerstiftung Nordrhein, Duesseldorf
CollaboratorUNKNOWN
Foerderinitiative Pharmazeutische Betreuung e.V., Berlin
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 old or older * patient admitted to one of the project wards * minimum hospitalization: 3 days * written informed consent (patient or the legal representative) * current medication of the patient at hospitalization

Exclusion criteria

* patients included in this study previously

Design outcomes

Primary

MeasureTime frame
Drug-related readmissionone year after discharge from the cooperating ward

Secondary

MeasureTime frameDescription
Number of prescribed potentially inappropriate medication (PRISCUS-criteria)during hospital stay on cooperating wards(continuous data collection during routine ward rounds;hence,duration of data collection is dependent on individual hospital stay of each patient, up to 1 year) and 1 year after discharge from the cooperating wardThe PRISCUS list was developed in 2010 for the German market. Potentially inappropriate medications were judged as inappropriate by an expert panel using the Delphi technique. \[Holt et al., Dtsch Arztebl 2010\]
time to readmissionone year after discharge from the cooperating ward
Number of accepted recommendations in the intervention groupduring hospital stay on cooperating wards (continuous data collection during routine ward rounds; hence, duration of data collection is dependent on individual hospital stay of each patient, up to one year) in the intervention group
Adverse drug eventsduring hospital stay on cooperating wards(continuous data collection during routine ward rounds;hence,duration of data collection is dependent on individual hospital stay of each patient, up to 1 year) and 1 year after discharge from the cooperating ward
drug-related problemduring hospital stay on cooperating wards (continuous data collection during routine ward rounds; hence, duration of data collection is dependent on individual hospital stay of each patient, up to one year) in the intervention group
number of changes in medication after dischargeone year
time for interventionduring hospital stay on cooperating wards (continuous data collection during routine ward rounds; hence, duration of data collection is dependent on individual hospital stay of each patient, up to one year) in the intervention grouptime recording for pharmaceutical care service

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026