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Recruiting Not applicable

Prioritising Patient Medication Review: Hospitals Reaching Out

NCT06451692 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2024-06-17
Last updated
2026-04-13

Condition(s) studied

Medication ReviewPolypharmacyGeneral PractitionersInterdisciplinary CommunicationClinical Pharmacy

Investigational drug(s) / intervention(s)

Clinical pharmacist

Clinical pharmacist: The clinical pharmacist calls the patients' GP 90 days after discharge for follow-up

Study summary

To examine the effect of a cross-sectoral medication review intervention to admitted multi-morbid, polypharmacy patients aged 65+ at SHS in two settings; an acute admission unit (typical admission time \< 48 hours) and a medical outpatient setting (patients routinely visits for follow-up, diagnosis or treatment, but do require a bed or overnight care).

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * all hospitalized patients who are prescribed at least seven medications specified in the Electronic Patient Journal (EPJ) at admission Exclusion Criteria: * terminal patients or patients with a short life expectancy, patients residing in another region, patients who are discharged on the day of inclusion, and finally patients who do not speak Danish.

Primary outcome measure(s)

  • Readmission and emergency department rate. — Up to thirty days after discharge
    The number of acute readmissions and emergency department visits between 4 hours and 30 days after discharge from the index hospital stay in the intervention group compared with the control group. As a "yes" or "no" and a time-to-event. Potential readmissions are assessed through the electronic patient journal.

Trial sites (1)

FacilityCityRegionStatus
Sygehus Sønderjylland Aabenraa Southern Denmark Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06451692 on ClinicalTrials.gov ↗ ← All trials in Denmark