Clinical Trials Directory

Trials / Withdrawn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Withdrawn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

TypeNameDescription
DRUGTopical SprayTopical spray containing Diclofenac 1.16%, Linseed Oil 3%, Menthol 5%, Methyl salicylate 10%.
DRUGTopical GelTopical gel containing Diclofenac 1.16%, Menthol 5%, Methyl salicylate 10%
OTHERSalineSaline

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.