Status:

RECRUITING

Comparison of Compounded Topical Anesthetics

Lead Sponsor:

Dartmouth-Hitchcock Medical Center

Conditions:

Procedural Pain

Eligibility:

All Genders

18-75 years

Phase:

PHASE4

Brief Summary

The primary objective for this pilot study is to evaluate the efficacy of the compounded topical anesthetic Benzocaine 20%/ Lidocaine 8%/Tetracaine 4% (BLT) compared to 4% Lidocaine topical in providi...

Eligibility Criteria

Inclusion

  • Men and women over 18, but not more than 75 years of age.
  • Patients who have a regularly scheduled dermatology appointment for Intense Pulse Light (IPL), Pulse Dye Laser (PDL), or microneedling.

Exclusion

  • Any subject who has a previous history of allergy, sensitivity, and contraindication to benzocaine, lidocaine, or tetracaine.
  • Patients with cardiac/respiratory disease, seizure disorder, or neuropathies.
  • Patients who are under treatment for a dermatologic condition that may interfere with the evaluation of the study.
  • Pregnant women and women who are breastfeeding.
  • Patients who report concurrent use of anxiolytics or opiates, which may interfere with the interpretation of results.

Key Trial Info

Start Date :

October 22 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2026

Estimated Enrollment :

64 Patients enrolled

Trial Details

Trial ID

NCT06569537

Start Date

October 22 2024

End Date

January 1 2026

Last Update

December 16 2025

Active Locations (1)

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Dartmouth Hitchcock Dermatology Clinic

Lebanon, New Hampshire, United States, 03766

Comparison of Compounded Topical Anesthetics | DecenTrialz