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Withdrawn Phase 2 Interventional

Study to Explore Effectiveness of Sublingual Fentanyl Spray in Emergency Department Patients With Acute Pain

ClinicalTrials.gov ID: NCT02137525

Public ClinicalTrials.gov record NCT02137525. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Multicenter, Double-Blind, Double Dummy, Active Comparator, Dose-Ranging Study to Explore the Efficacy of SUBSYS® in Emergency Department Patients With Acute Pain

Study identification

NCT ID
NCT02137525
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 2
Lead sponsor
INSYS Therapeutics Inc
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

  • Morphine 6 mg Drug
  • Fentanyl 100 µg Drug
  • Fentanyl 200 µg Drug
  • Fentanyl 400 µg Drug
  • Placebo Sublingual Spray Drug
  • Intravenous Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Jun 28, 2017
Completion
Not listed
Last update posted
Jul 4, 2017

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
13
Facility City State ZIP Site status
Maricopa Medical Center Phoenix Arizona 85008
Olive View-UCLA Medical Center Sylmar California 91342
Kansas University Medical Center Kansas City Kansas 66160
Henry Ford Hospital Detroit Michigan 48021
Wayne State University School of Medicine Detroit Michigan 48201
Hennepin County Medical Center Minneapolis Minnesota 55415
Washington University St Louis Missouri 63110
Stony Brook University HSC Stony Brook New York 11794
Duke University School of Medicine Durham North Carolina 27710
University of Cincinnati Cincinnati Ohio 45267
Pennsylvania Hospital Philadelphia Pennsylvania 19107
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107
Vanderbilt University Nashville Tennessee 37232
Baylor College of Medicine Houston Texas 77030
University of Virginia Health System Charlottesville Virginia 22908

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02137525, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 4, 2017 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02137525 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →