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Clinical Trials/NL-OMON36046
NL-OMON36046CompletedNot Applicable

Preventive Methods for Reduction of Pain associated with Propofol Injection: a randomised controlled trial of commonly used methods - Preventive Methods for Reduction of Pain associated with Propofol Injection

Catharina-ziekenhuis0 sites436 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
436

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • ASA 1 and 2 patients, aged 18-80 years, who will undergo an elective surgical procedure under general anaesthesia

Exclusion Criteria

  • use of NSAIDs or opiates on a regular basis or if communication of psychological disorders are present. Further exclusion criteria are history of polyneuropathy, pre-existing underlying pathology associated with pain, known hypersensitivity to lidocaine, propofol, lipid emulsions, egg or egg products, emergency surgery, pregnancy and patients using antidepressant medications

Investigators

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