Comparison of Compounded Topical Anesthetics
- Conditions
- Procedural Pain
- Registration Number
- NCT06569537
- Lead Sponsor
- Dartmouth-Hitchcock Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not yet recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria:<br><br> - Men and women over 18, but not more than 75 years of age.<br><br> - Patients who have a regularly scheduled dermatology appointment for Intense Pulse<br> Light (IPL), Pulse Dye Laser (PDL), or microneedling.<br><br>Exclusion Criteria:<br><br> - Any subject who has a previous history of allergy, sensitivity, and contraindication<br> to benzocaine, lidocaine, or tetracaine.<br><br> - Patients with cardiac/respiratory disease, seizure disorder, or neuropathies.<br><br> - Patients who are under treatment for a dermatologic condition that may interfere<br> with the evaluation of the study.<br><br> - Pregnant women and women who are breastfeeding.<br><br> - Patients who report concurrent use of anxiolytics or opiates, which may interfere<br> with the interpretation of results.
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain as measured by the Numeric Pain Rating Scale (NPRS);Pain as measured by the Wong-Baker Face Pain Rating Scale
- Secondary Outcome Measures
Name Time Method