Expired Study
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Hartford, Connecticut 06106


Purpose:

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 from 30 minutes to 5 minutes. The child's pain with the blood drawing procedure is evaluated.


Criteria:

Inclusion Criteria: - Ages 3-7, requiring venipuncture Exclusion Criteria: - Emergent procedure - Allergy to lidocaine or sodium lauryl sulfate


NCT ID:

NCT00126932


Primary Contact:

Principal Investigator
William T. Zempsky, MD
CT Children's Medical Center


Backup Contact:

N/A


Location Contact:

Hartford, Connecticut 06106
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 16, 2017

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