ACTRN12608000414314
Completed
Phase 4
A randomised clinical trial to compare the efficacy of pressurised vapocoolant spray and subcutaneous lignocaine injection in decreasing the pain of intravenous cannulation in the emergency department
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Austin Health
- Enrollment
- 220
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Emergency department patients, aged 18 years or more, requiring intravenous cannulation
Exclusion Criteria
- •Refusal to provide consent
- •Inability to provide informed consent (Non\-English speaking, altered mental state, significant illness, urgent need for IV cannulation)
- •Moderate to severe discomfort or pain
- •Diseases of the skin associated with cold intolerance (eg: Raynaud’s)
- •Known allergy to spray contents or lignocaine
- •Peripheral neuropathy
- •Parenteral analgesia in the previous 4 hours
- •Use of other local anaesthetics
Outcomes
Primary Outcomes
Not specified
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