Status:

WITHDRAWN

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

Lead Sponsor:

Banner Health

Conditions:

Wounds

Eligibility:

All Genders

18-75 years

Phase:

NA

Brief 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.

Detailed 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 m...

Eligibility Criteria

Inclusion

  • Signed and dated consent form \& HIPAA
  • \>/= 18 yo
  • Single stage 2-3 wound evaluated by our wound care team
  • Alert and oriented (thinking ability clear and intact, physician approval)
  • English language proficiency, likely to be able to participate in all scheduled evaluations

Exclusion

  • Allergy to morphine, codeine, or versa base
  • pts taking medications for acute condition, other than for the wound pain (can be taking chronic pain meds if current dose stable for past 3 mo)
  • Patients with neuropathies
  • Patients with respiratory conditions
  • Patients that are pregnant

Key Trial Info

Start Date :

April 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2010

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT00755989

Start Date

April 1 2009

End Date

April 1 2010

Last Update

July 20 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Banner Good Samaritan Medical Center

Phoenix, Arizona, United States, 85006

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