Comparison of Synera Patch Versus LMX-4 Cream Versus Placebo Patch for Pain Reduction During Venipuncture in Children
Launched by CAROL MORREALE · May 3, 2010
Trial Information
Current as of July 21, 2025
Completed
Keywords
ClinConnect Summary
This study will compare the effectiveness of a patch applied for 30 minutes (Synera-lidocaine 70 mg/tetracaine 70 mg) with the effectiveness of a cream (LMX-4- 4% liposomal lidocaine) and a placebo patch applied for the same length of time in reducing pain due to needle sticks in children. One hundred fifty children and adolescents 5-17 years old admitted to emergency department or presenting to the phlebotomy lab. will be randomly placed in each group. Children will rate their level of pain using the Faces Pain Scale-Revised (FPS-R) before the medication is applied, after the medication is...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Children requiring venipuncture for medical care
- • The ability to demonstrate proper understanding of the Faces Pain Scale-Revised (FPS-R)
- • Parents of enrolled children need to be present during the procedure and be willing to rate their child's pain
- Exclusion Criteria:
- • Damaged or inflamed skin at the designated application site
- • Known sensitivity to components of Synera or LMX-4 (lidocaine, tetracaine, or local anesthetics of the amide or ester type, PABA derivatives)
- • Contraindications to Synera or LMX-4 use (severe hepatic disease, history of drug-induced methemoglobinemia, taking Class 1 antiarrhythmics)
- • Use of analgesics during the past 24 hours
- • Teenage female participants who are pregnant or lactating
- • If in the attending's judgment the patient cannot wait wait 30 minutes for a blood drawn. These conditions include but are not limited to: sepsis, trauma, surgical emergencies, severe dehydration.
About Carol Morreale
Carol Morreale is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes. With a strong focus on innovative therapeutic solutions, Ms. Morreale oversees the design, implementation, and management of clinical trials across various therapeutic areas. Her expertise in regulatory compliance, patient safety, and data integrity ensures that all trials are conducted to the highest ethical and scientific standards. Passionate about fostering collaboration among research teams, healthcare professionals, and stakeholders, Carol Morreale strives to bring cutting-edge treatments from the laboratory to the clinic, ultimately enhancing the quality of care for patients.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Charleston, West Virginia, United States
Patients applied
Trial Officials
James M. Turner, DO
Principal Investigator
Charleston Area Medical Center, Emergency Department
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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