Pain Clinical Trial
Official title:
A Randomized, Double-Blind, Placebo Controlled, Paired Study Evaluating S-Caine™ Peel (Lidocaine 7% and Tetracaine 7% Cream) for Induction of Local Dermal Anesthesia for Laser-Assisted Tattoo Removal in Adults
| Verified date | September 2005 |
| Source | ZARS Pharma Inc. |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Food and Drug Administration |
| Study type | Interventional |
There is pain associated with laser-assisted tattoo removal. For this reason, some form of anesthesia is commonly used to eliminate or minimize the pain. This anesthesia is usually a topical local anesthetic cream or ointment spread over the skin. The purpose of this study is to further estimate the effectiveness of S-Caine™ Peel (lidocaine 7% and tetracaine 7% cream) for treating pain during laser-assisted tattoo removal.
| Status | Completed |
| Enrollment | 60 |
| Est. completion date | September 2005 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Patient is 18 years of age or older - Patient elects to undergo laser-assisted tattoo removal Exclusion Criteria: - Patient is pregnant or breastfeeding - Patient has participated in a clinical trial of an unapproved drug within the previous 30 days - Patient has participated in any previous clinical trial involving S-Caine Peel |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Masking: Double-Blind, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | Laser and Skin Surgery Center of New York | New York | New York |
| Lead Sponsor | Collaborator |
|---|---|
| ZARS Pharma Inc. |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | To evaluate the efficacy of S-Caine Peel when applied for 60 minutes for induction of local dermal anesthesia prior to laser-assisted tattoo removal in adults | |||
| Secondary | To monitor the nature and frequency of adverse events (AEs) associated with the application of S-Caine Peel |
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