Intranasal Fentanyl for Pain Management

Status unconfirmed · Phase 4

Conditions studied: Trauma, Pain

In brief

Goal of the research will be to demonstrate a reduction in reported pain following the atomization and intra-nasal administration of Fentanyl versus the reduction in pain achieved from intravenous Fentanyl. It is hypothesized that pain should be reduced following fentanyl administration using the intra-nasal atomization equal to the intravenous delivery.

Key facts

Study ID

NCT00882960

Run by

Genesys

People needed

500

Starts

2009-04-01

Expected to finish

2012-04-01

Last updated by the study team

2011-05-04

Who can join

Age: 14 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Persons who meet the current State of Michigan County of Oakland and County of Genesee pre-hospital pain requiring analgesia.
• Examples of these patients would be those with fractures, kidney stones, or traumatic injuries, burns.

You may not qualify if…

• Patients who have compromised nasal pharynx such as those who have obvious fractures or epistaxis.
• Additionally patients who are in the supine position for cervical spine immobilization will be excluded.

Where it is running

• Genesys Regional Medical Center — Grand Blanc, Michigan, United States (enrolling)

Full record on ClinicalTrials.gov

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