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Clinical and Economical Assessment of an Intervention to Reduce Potentially Inappropriate Medication in Polymedicated Elderly Patients

Clinical and Economical Assessment of an Intervention to Reduce Potentially Inappropriate Medication in Polymedicated Elderly Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02275572
Acronym
REMEI
Enrollment
503
Registered
2014-10-27
Start date
2012-03-31
Completion date
Unknown
Last updated
2014-10-27

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

Conditions

Elderly, Polypharmacy

Brief summary

Objective: To evaluate the clinical and economic impact of the application of an algorithm to improve the adequacy and safety of pharmacotherapy in elderly polymedicated (receiving 8 or more medications), not institutionalized. Design: randomized, open, multicenter and two branches of parallel intervention clinical trial. Intervention Study: primary care pharmacist apply the GP-GP algorithm to each drug with the support of STOPP criteria, Beers and / or recommendations CatSalut. The pharmacist submit to doctor his findings and reach a consensus and decide which recommendations will be presented to patient. Control intervention: usual procedure. Main outcome measures: a) Discontinued medications, changed or changing doses, b) GP consultations, hospital emergency department and hospital admissions for acute illness, c) pharmaceutical expenditure, d) restart medication e) complications underlying diseases. Follow-up control at 1 month (security) and at 3, 6 and 12 months.

Interventions

Sponsors

Consorci Sanitari del Maresme
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* 70 years or more * Currently receiving eight or more drugs, except ointments and administered via topical nonprescription * Give their informed written consent to participate in the study.

Exclusion criteria

* Estimated life expectancy less than 6 months. * Active cancer * Participation in any other clinical trial or program for evaluation of medication in the elderly. * Institutionalized in nursing homes. * Surgical intervention scheduled for the next 6 months

Design outcomes

Primary

MeasureTime frame
Number of patients with medications discontinued, reduced dose or changed.baseline, 3, 6 and 12 months
Number of discontinued medications, changed or changing doses.baseline, 3, 6 and 12 months

Secondary

MeasureTime frameDescription
Quality of lifebaseline, 3 and 6 monthsEuroQoL questionnaire
Pharmaceutical recommendations acceptance ratebaseline
Resumption of medication3, 6 and 12 months
Mortality3, 6 and 12 months
Healthcare resource consumption3, 6 and 12 monthsNumber of visits to Primary care center, Number of visits to hospital emergency department, Number of hospital admission, Number of outpatients hospital visits.
Medication adherencebaseline, 3 and 6 monthsMorisky-Green questionnaire

Outcome results

None listed

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