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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON36046

Enrollment

436

Registered

2011-08-10

Start date

2011-06-01

Completion date

Unknown

Last updated

2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Injection

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Our primary goal is to try and establish the most effective and easy to use method for preventing PIP, without slowing induction of anaesthesia.	—

Secondary

Measure	Time frame
Secondary goal is to try and find a correlation between pain on IV-cannulation and the experience of PIP.	—

Countries

Netherlands

Outcome results