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COMPLETEDPhase 3NCT05288348

DSUVIA Early Evaluation of Pain Trial

Randomized, interventional trial of Emergency Department (ED) administration of DSUVIA (sufentanil) versus standard care pain management comparing pain treatment outcomes in injured patients with mode...

Lead sponsor: Frank Guyette•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Frank Guyette

Collaborators

United States Department of Defense

Age

18 - 70 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•1. Trauma activation (Level I, II or III)
•2. Age 18-70 years inclusive
•3. Need for pain treatment based upon NRS (0-100) clinical pain measurement ≥ 50
•4. Estimated time in Emergency Department \> 30 minutes following informed consent

Exclusion Criteria

•1. Advanced airway management prior to 1st dose administration
•2. Known allergy to opioids
•3. Known prisoner
•4. Known pregnancy
•5. ED pain medication contraindicated
•6. Significant respiratory depression
•7. Known or suspected gastrointestinal obstruction, including paralytic ileus

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: April 30, 2025Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE3

Enrollment150

Start dateAug 2022

Last updatedApr 30, 2025

Condition

Traumatic Injury

Locations shown

University of Pittsburgh

Pittsburgh, Pennsylvania

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 30, 2025Data synced to Clareo: May 16, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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