Validation of methods for monitoring nociception and pain prediction in the IC

Recruiting

• Conditions: Other chronic pain; R52.0; R52.2; Acute pain

• Registration Number: DRKS00011206
• Lead Sponsor: Arbeitsgruppe „Anästhesiologische und analgesiologische Neurophysiologie, Klinik für Anästhesiologie m.S. operative Intensivmedizin, Campus Charité Mitte und Campus Virchow Klinikum, Charité - Universitätsmedizin Berlin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-01-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 1100

Inclusion Criteria

mechanically ventilated patients in intensive care units
- unable to communicate pain level due to sedation or impared consciousness
- potentially painfull diagnostic or therapeutic interventions during routine care

Exclusion Criteria

none

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Difference in duration of mechnical ventilation between sedated intensive care patients showing nociceptive reactions to painful procedures compared to similar patients without nociceptive reactions.