Trials / Recruiting
RecruitingNCT06569537
Comparison of Compounded Topical Anesthetics
Comparison of Compounded Topical Anesthetics for Pain Relief of Intense Pulsed Light, Pulse Dye Laser, and Microneedling Treatments
- Status
- Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 64 (estimated)
- Sponsor
- Dartmouth-Hitchcock Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
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 providing relief of pain during IPL, PDL, and microneedling procedures.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine topical | 4% |
| DRUG | BLT | Topical Benzocaine 20%/ Lidocaine 8%/Tetracaine 4% |
Timeline
- Start date
- 2024-10-22
- Primary completion
- 2026-01-01
- Completion
- 2026-01-01
- First posted
- 2024-08-26
- Last updated
- 2025-12-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT06569537. Inclusion in this directory is not an endorsement.