Status:
COMPLETED
Reduction of Topical Anesthetic Onset Time Using Ultrasound
Lead Sponsor:
Connecticut Children's Medical Center
Conditions:
Pain
Eligibility:
All Genders
3-7 years
Phase:
PHASE4
Brief Summary
Children ages 3-7 who are undergoing blood drawing receive either standard care, topical medicine for numbing (LMX4), or the study intervention which utilizes ultrasound to speed the onset of LMX4 fro...
Eligibility Criteria
Inclusion
- Ages 3-7, requiring venipuncture
Exclusion
- Emergent procedure
- Allergy to lidocaine or sodium lauryl sulfate
Key Trial Info
Start Date :
October 1 2004
Trial Type :
INTERVENTIONAL
End Date :
December 1 2004
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT00126932
Start Date
October 1 2004
End Date
December 1 2004
Last Update
December 27 2007
Active Locations (1)
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1
CT Children's Medical Center
Hartford, Connecticut, United States, 06106