Trials / Withdrawn
WithdrawnNCT02400320
Local Skin Safety Study of a Topical Pain Relief Spray Containing a Combination of Diclofenac, Methyl Salicylate, and Menthol
Cumulative Skin Irritation Study Evaluating the Skin Irritancy Potential of Topical Analgesic Vovilup Spray Containing a Combination of Diclofenac, Menthol, Methyl Salicylate and Linseed Oil and Comparing it With a Marketed Formulation - Iodex Ultragel
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- GlaxoSmithKline · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to determine local skin safety of a topical analgesic spray containing a combination of diclofenac, methyl salicylate, menthol and compare it with a topical analgesic gel containing a combination of diclofenac, methyl salicylate, and menthol.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Topical Spray | Topical spray containing Diclofenac 1.16%, Linseed Oil 3%, Menthol 5%, Methyl salicylate 10%. |
| DRUG | Topical Gel | Topical gel containing Diclofenac 1.16%, Menthol 5%, Methyl salicylate 10% |
| OTHER | Saline | Saline |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2016-06-01
- Completion
- 2016-06-30
- First posted
- 2015-03-27
- Last updated
- 2017-09-12
Source: ClinicalTrials.gov record NCT02400320. Inclusion in this directory is not an endorsement.