drugset / Trial / NCT01821274
A 21-Day Topical Safety Study of Diltiazem Hydrochloride Using a Cumulative Irritant Patch Test Design
RandomizedSingle-groupTriple-blindTreatment
Summary
The purpose of the study is to determine whether Diltiazem Hydrochloride 2% Cream will cause irritation to skin on the back of healthy volunteers after repeated application over 21-days.
Timeline
- Start
- 2013-03
- Primary completion
- 2013-07
- Completion
- 2013-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Diltiazem | Small molecule | 2 % | Topical |
| Subject | Diltiazem | Small molecule | 0.2 g | Topical |
| Comparator | Sodium Lauryl Sulfate | Small molecule | 0.1 % | Topical |
| Comparator | Sodium Lauryl Sulfate | Small molecule | 0.2 ml | Topical |