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Objective evaluation of sedation, pain and delirium in palliative care patients in a nursing home; pilot study

Objective evaluation of sedation, pain and delirium in palliative care patients in a nursing home; pilot study - Evaluation of sedation, pain and delirium in palliative care; pilot

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31858
Enrollment
10
Registered
2008-07-23
Start date
2008-08-11
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

palliatieve zorg comfort sedation

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients in terminal stages of illness at palliative unit in nursing home Laurens, Antonius IJsselmonde, Rotterdam; informed consent

Exclusion criteria

Exclusion criteria: no informed consent; time too short to take a BIS score before sedation

Design outcomes

Primary

MeasureTime frame
Primary research question: Can comfort be monitored in palliative care patients in a nursing home by measuring sedation, pain and delirium?

Secondary

MeasureTime frame
Secundary research question: Is the Bispectral index (BIS) monitor valid to measure depth of sedation in palliative care patients in a nursing home and associated with the given medication? Is a change in BIS score correlated to a change in medication given to influence the depth of sedation?

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)