Preventive Methods for Reduction of Pain associated with Propofol Injection: a randomised controlled trial of commonly used methods
Completed
- Conditions
- Pain Injection10001316
- Registration Number
- NL-OMON36046
- Lead Sponsor
- Catharina-ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 436
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
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Our primary goal is to try and establish the most effective and easy to use<br /><br>method for preventing PIP, without slowing induction of anaesthesia. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary goal is to try and find a correlation between pain on IV-cannulation<br /><br>and the experience of PIP. </p><br>