PENTHROX™ in the Canadian Emergency Department (ED)

PHASE4CompletedINTERVENTIONAL
Enrollment

99

Participants

Timeline

Start Date

April 8, 2019

Primary Completion Date

March 30, 2020

Study Completion Date

September 8, 2020

Conditions
Pain, Acute
Interventions
DRUG

Methoxyflurane 3mL

As soon as possible following enrollment and initial procedures, the patient will be supplied with a PENTHROX™ kit which includes one inhaler containing 3 mL of MEOF for pain management. A member of the research team will train the patient to self-administer MEOF. PENTHROX™ is an approved (trademarked) product in Canada and is commercially available in a combination blister pack with one 3 mL sealed bottle and one PENTHROX™ inhaler with the Activated Carbon (AC) chamber.

Trial Locations (6)

B3H3A7

Charles V Keating Emergency and Trauma Centre, QEII, Halifax

L4M 6M2

Royal Victoria Regional Health Centre, Barrie

L3P 7P3

Markham Stouffville, Markham

L3B4W6

St. Joseph's Healthcare, Welland

G7H 7K9

Centre Integre Universitaire De Sante Et De Service Sociaux (CIUSSS) Saguenay-Lac-Saint Jean, Chicoutimi

J4V 2H1

Centre Intégré de Santé et de Services Sociaux de la Montérégie-Centre, Greenfield Park

All Listed Sponsors
lead

Purdue Pharma, Canada

INDUSTRY

NCT03868436 - PENTHROX™ in the Canadian Emergency Department (ED) | Biotech Hunter | Biotech Hunter