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Appropriate medication use in Dutch terminal care: AMUSE TRIAL

Appropriate medication use in Dutch terminal care: AMUSE TRIAL - The Dutch medication optimisation trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON54289
Enrollment
250
Registered
2022-01-27
Start date
2022-04-29
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

patiënten met een levensverwachting van drie maanden of minder, ongeacht hun onderliggend lijden. Patients with a limited life expectancy

Interventions

We will evaluate the effect of a weekly (personalized) medication advice on adequate medication management in patients in the last phase of life provided by CDSS-OPTIMED. The advice is based on curr

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. The patient is 18 years or over and provides informed consent to participate. 2. The patient is aware that recovering from his/her disease is unlikely, as assessed by the attending physician. 3. The patient is competent to decide about trial participation 4. The patient has a life expectancy of at least two weeks and at most three months, as estimated by an attending physician.

Exclusion criteria

Exclusion criteria: 1. The patient is incapable of filling in a (Dutch) questionnaire (patients may be supported by relatives when filling in the questionnaire).

Design outcomes

Primary

MeasureTime frame
Patients* quality of life two weeks after baseline assessment, as measured by the EORTC QLQ-C15-PAL questionnaire (scale 0 to 100).

Secondary

MeasureTime frame
• Patients* quality of life at day 7, 21, 28, and then every 28 days until death (or as long the patient is able to fill in the questionnaire), as measured by the EORTC QLQ-C15-PAL questionnaire (scale 0 to 100), quality of life question. • Symptoms and the occurrence of potential side effects of continuing or discontinuing medication at day 1-7, 14, 21, 28, and then every 28 days until death, as assessed by the Utrecht Symptoom Dagboek (USD, which is based on the Edmonton Symptom Assessment Scale (ESAS), frequently used in palliative care and available in most electronic patient records; • Blood pressure and glucose level in case of antihypertensives and antidiabetics (continued or discontinued) at day 1-7, 14, 21, 28, and then every 28 days until death; for patients discharged to or staying at home the attending home care service will be asked to perform these measurements; • Thrombo-embolic and bleeding events; • Time spent on discussing the medication with the patient, as registered on a time scale (0-5 minutes, 6-10, 11-15 minutes, etc.); • Health care costs, including medication prescriptions, hospital admissions and in-hospital care; • Medication used until death, as derived from patients* medical records and the pharmacist*s information system; • Survival from the moment of inclusion.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)