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Pain monitor in the intensive care medicine

Pain monitor in the intensive care medicine - Schmemo

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00003062
Enrollment
140
Registered
2011-08-08
Start date
2010-08-13
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Analgo-sedated patients in the ICU

Interventions

Group 1: The RIII-reflex threshold is measured preoperatively to obtain baseline values for each individual patient. Therefore the RIII-reflex is stimulated via surface electrodes over the sural nerve

Sponsors

Charité Universitätsmedizin Berlin Klinik für Anästhesiologie Campus Charité Mitte
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: legal age, patients that receive surgery for which a postoperative sedation is planed. Patients have to give consent preoperatively.

Exclusion criteria

Exclusion criteria: Damages or severe Neuropathies of peripheral nerves of the lower limb, Patients with ICD or pacemaker.

Design outcomes

Primary

MeasureTime frame
Predictability of Behavioral pain scale score >6 by using the RIII-Reflex threshold

Secondary

MeasureTime frame
Predictability of inadequate analgesia defined as an NRS>4 in awake ICU patients by using the RIII-reflex threshold

Countries

Germany

Contacts

Public ContactJan H. Baars

Charité Campus Charité Mitte

jan.baars@charite.de+49 30 450 531227

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 27, 2026