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Topical Amethocaine versus Topical Eutectic Mixture of Local Anaesthetic (EMLA)

In Children's Emergency does topical Amethocaine 4% increase cannulation success compared to Topical Eutectic Mixture of Local Anaesthetic (EMLA) 5%?

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000409572
Acronym
TAVE
Enrollment
660
Registered
2006-09-19
Start date
2006-11-15
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Children's distress and pain from intravenous cannulation is reduced with the use of topical anaesthetic cream. At Starship children’s emergency department (CED) we use EMLA (Eutectic Mixture of Local Anaesthetic) and are very satisfied with its effect. A recent Cochrane systematic review suggests that Amethocaine is a better topical anaesthetic (1). Amethocaine works faster and has better pain relieving abilities than EMLA independent of application time. There is even a suggestion that Amethocaine may improve success rates for IV access although the evidence was inconclusive. EMLA is a vasoconstrictor, which appears to constrict veins whereas Amethocaine is a vasodilator and causes local erythema. Amethocaine has traditionally been more expensive than EMLA. The Cochrane review found two clinical questions unanswered; does Amethocaine improve cannulation success rate and what are the cost implications? This research project will attempt to answer these questions by comparing the use of EMLA and Amethocaine for topical anaesthesia in children undergoing intravenous cannulation at Starship CED. 1. Lander JA, Weltman BJ and So SS. EMLA and Amethocaine for reduction of children’s pain associated with needle insertion (Review). Cochrane Database of Systematic Reviews. (3). 2006.

Interventions

Intervention is Amethocaine, in a single dose of 1-2g in two places. The two sites are typically on the dorsum of both hands, but may include other sites depending on the triage nurses judgement. Study runs from November 2006 until March 2007.

Sponsors

Auckland District Health Board
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
0 to 14 Years
Healthy volunteers
No

Inclusion criteria

All children having topical anaesthetic applied for intravenous cannulation in our department are eligible.

Exclusion criteria

Those needing emergency IV access or contraindications to topical anaesthetic (currently <3 months of age or on met-Haemaglobinaemia inducing medicines).

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 31, 2026