MedTrace Logo

Sublingual Fentanyl and Procedural Burn Pain

NCT02241486 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2017-07-28

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to examine the efficacy and safety of sublingual fentanyl spray (Subsys) for procedural pain (dressing changes/minor debridement) in patients with burn injury.

Conditions

  • Burn Pain

Interventions

DRUG

Sublingual Fentanyl Spray

Patients with burn injuries will receive sublingual fentanyl spray (Subsys) for procedural pain (dressing changes/minor debridement).

Sponsors & Collaborators

  • Loyola University

    lead OTHER

Principal Investigators

  • Joseph R Holtman Jr, MD Ph.D. · Department Anesthesiology Loyola University Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-09-30
Completion
2015-03-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02241486 on ClinicalTrials.gov