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Use of Morphine Gel Topically in Patients With Stage 2-3 Wounds

Wounds Clinical Trial

Official title:
A Phase 3, Single-Centered, Randomized, Double-Blind, Placebo-Controlled, Efficacy and Safety Trial of Morphine Sulfate Gel 0.1% in Patients With Stage 2-3 Wounds

Clinical Trial Summary

Morphine gel applied topically to wounds will reduce wound pain and decrease patients use of oral and intravenous pain medications, therefore reducing side effects.

Clinical Trial Description

Patients will be randomized to receive either placebo (versa base gel) or morphine gel to wound. Patients receiving morphine gel will have a decrease in pain score and use less oral/intravenous pain medications. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00755989
Study type Interventional
Source Banner Health
Contact Mary Whitmer, FNP
Phone 602-239-6078
Email marywhitmer@bannerhealth.com
Status Not yet recruiting
Phase Phase 3
Start date December 2008
Completion date December 2009
View Details
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