Viewing Study NCT00441051



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Study NCT ID: NCT00441051
Status: COMPLETED
Last Update Posted: 2007-02-28
First Post: 2007-02-27

Brief Title: Efficacy and Safety of Diclofenac Sodium 01 Gel in Patients With UV Induced Painful Sunburn
Sponsor: Novartis
Organization: Novartis

Study Overview

Official Title: A Randomized Double-Blind Vehicle-Controlled Single Center Intra-Individual Comparative Study of the Efficacy and Safety of Diclofenac Sodium 1 mgg 01 Gel in Subjects With Painful UV-Induced Erythema
Status: COMPLETED
Status Verified Date: 2007-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Diclofenac sodium 01 will be applied to sunburned skin when the intensity of pain reaches a certain level in order to evaluate the efficacy and safety of the treatment on this induced pain
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None