Patient-centred Deprescribing of Psychotropic, Sedative and Anticholinergic Medication in Elderly Patients With Polypharmacy

Recruiting N/A Interventional Study
Deprescriptions Antidepressive Agents Antipsychotic Agents Analgesics, Opioid Hypnotics and Sedatives Cholinergic Antagonists
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
65 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
352 (estimated)
Sponsor
Ludwig-Maximilians - University of Munich · Other
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About This Trial
The PARTNER study is a multicentre, two-arm, pragmatic cluster-randomised trial evaluating the impact of a focused and patient-centred cooperation between general practitioners (GPs) and community pharmacists (PARTNER intervention) on reductions in the use of psychotropic, sedative and anticholinergic potentially inappropriate medication (PSA-PIM) compared to a control intervention. The PARTNER in…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Aged 65 years or older * Patient is capable of giving consent * GP contact in the quarter prior to inclusion * Current use of ≥ 5 drugs, including ≥ 1 PSA-PIM (hypnotics, opioids, gabapentinoids, antipsychotics, antidepressants, anticholinergic urospasmolytics) with a treatmen…
Contacts

Tobias Dreischulte, Prof. Dr.

+49 89 4400 55447

tobias.dreischulte@med.uni-muenchen.de

CONTACT

Annette Haerdtlein

+49 89 4400 54976

annette.haerdtlein@med.uni-muenchen.de

CONTACT