Clinical trial
Efficacy and Safety of Diclofenac Sodium (0.1%) Gel in Patients With UV Induced…
NCT00441051 · Novartis, Industry · Completed
Key facts
| NCT number | NCT00441051 |
|---|---|
| Title | Efficacy and Safety of Diclofenac Sodium (0.1%) Gel in Patients With UV Induced Painful Sunburn |
| Official title | A Randomized, Double-Blind, Vehicle-Controlled, Single Center, Intra-Individual Comparative Study of the Efficacy and Safety of Diclofenac Sodium 1 mg/g (0.1%) Gel in Subjects With Painful UV-Induced Erythema |
| Lead sponsor | Novartis, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Sunburn |
| Intervention type | Drug |
| Interventions | Diclofenac sodium 1mg/g |
| Enrollment | 45 |
| Start date | Nov 1, 2006 |
| Completion | Dec 1, 2006 |
| First posted | Feb 28, 2007 |
| Last update posted | Feb 28, 2007 |
| Countries | France |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: