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Clinical Trials/DRKS00021149
DRKS00021149
Completed
Not Applicable

Recording the level of analgesia in intensive care patients - is the measurement of the RIII-reflex a useful addition to the established categorical pain detection scales in non-communicative patients?

Klinik für Anästhesiologie - Interdisziplinäre Operative Intensivmedizin0 sites144 target enrollmentMarch 26, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Detection of the nociceptive flexor reflex in the analgosedated intensive care patientIncidence of deliriumMortality ratesAssessment of the thresholds in different subgroups
Sponsor
Klinik für Anästhesiologie - Interdisziplinäre Operative Intensivmedizin
Enrollment
144
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 26, 2020
End Date
March 20, 2020
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Klinik für Anästhesiologie - Interdisziplinäre Operative Intensivmedizin

Eligibility Criteria

Inclusion Criteria

  • Men and women aged\> 18 years
  • At the time of data collection, the patient is ventilated and analgosedated
  • Post\-hoc information or consent from the patients legal designees

Exclusion Criteria

  • age \<18 years
  • neurological diseases that are associated with a restriction of peripheral conduction, such as
  • Cross\-sectional symptoms
  • muscular dystrophy
  • polyneuropathy (also in advanced diabetes mellitus, C2 abuse)
  • Critical illness polyneuropathy (CIP) \- clinical suspicion,
  • Multiple sclerosis, Guillain\-Barré syndrome, denervating neurological
  • Cardiac pacemakers or electrical defibrillators \- so far no damage to such devices has been demonstrated by the applied currents. We want to avoid any potential damage to the devices and thus endanger the patient!
  • subsequently withdrawn consent to study participation
  • Patients who have already been included in the study and who have to be re\-admitted to the intensive care unit after transfer from the ICU will not be included in the study again.

Outcomes

Primary Outcomes

Not specified

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