Nociception Level monitoring in the Intensive Care

Nociception Level monitoring in the Intensive Care - an observational cohort study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON25056

Enrollment

Registered

2020-12-17

Start date

2020-12-28

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Intensive care patients Mechanical ventilation Pain in sedated patients

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: - Aged 18 years or older - Mechanical ventilation for any reason - Deemed suitable by the investigators

Exclusion criteria

Exclusion criteria: - Aged 17 years or younger - Not deemed suitable by the investigators

Design outcomes

Primary

Measure	Time frame
- NOL index values up to 8 hours	—

Secondary

Measure	Time frame
- Blood pressure and heart rate; - Drug administration; - Nociceptive events will be collected on the eCRF; - Patient age, sex and underlying condition.	—

Contacts

Public ContactImeen van der Wal

Leiden University Medical Center

l.i.van_der_wal@lumc.nl0623203838

Outcome results