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Clinical Trials/ACTRN12606000121561
ACTRN12606000121561
Completed
Not Applicable

A randomised clinical trial to compare the efficacy of Eutectic Mixture of Local Anaesthetics (EMLA) and nitrous oxide (N2O) in decreasing the pain of intravenous cannulation in children

orthern Hospital, VIC0 sites100 target enrollmentApril 4, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
orthern Hospital, VIC
Enrollment
100
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 4, 2006
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
orthern Hospital, VIC

Eligibility Criteria

Inclusion Criteria

  • Required IV cannulation or venepuncture.

Exclusion Criteria

  • They were excluded if allergy to EMLA or nitrous oxide, suspected pneumothorax, bowel obstruction or other trapped gas, or if the parent/guardian are non\-English speaking. Patients also need to be able to wait at least thirty minutes prior to cannulation.

Outcomes

Primary Outcomes

Not specified

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