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Clinical Trials/ACTRN12619001596190
ACTRN12619001596190
Not yet recruiting
未知

Does intraoperative monitoring of the nociception level index (NOL) allow a prediction of the severity of acute postoperative pain?

Thomas Ledowski0 sites80 target enrollmentNovember 20, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
acute pain
Sponsor
Thomas Ledowski
Enrollment
80
Status
Not yet recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 20, 2019
End Date
TBD
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Adult patients (both sexes) scheduled for non\-emergency surgery under general anaesthesia with opioid/sevoflurane at the Royal Perth Hospital

Exclusion Criteria

  • Patients will be excluded from further analysis if they lack sufficient English language skills to consent and/or to communicate pain on a self\-rated pain scale, have a condition or medication known or suspected of interacting with the acquisition of the data (i.e. know severe peripheral neuropathy, known severe mental disorder), chronic pain (with opioid medication at home), use of ketamine at home, abuse of amphetamines or opioids, allergy to sticky tape.

Outcomes

Primary Outcomes

Not specified

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