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
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Catharina-ziekenhuis
- 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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