ACTRN12607000470493
Completed
Phase 3
A randomised controlled clinical trial to compare the efficacy of pressurised vapocoolant and water sprays in decreasing the pain of intravenous cannulation in emergency department patients.
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Pain of intravenous cannulation
- Sponsor
- Austin Health
- Enrollment
- 200
- 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); Moderate to severe discomfort or pain; Diseases of the skin associated with cold intolerance (eg: Raynaud’s phenomenon); Known allergy to spray contents; Peripheral neuropathy; Parenteral analgesia in the previous 4 hours
Outcomes
Primary Outcomes
Not specified
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Unknown
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