Ontology highlight
ABSTRACT: Aims
To measure and evaluate clinical response to nasal naloxone in opioid overdoses in the pre-hospital environment.Design
Randomised, controlled, double-dummy, blinded, non-inferiority trial, and conducted at two centres.Setting
Participants were included by ambulance staff in Oslo and Trondheim, Norway, and treated at the place where the overdose occurred.Participants
Men and women age above 18 years with miosis, rate of respiration ≤8/min, and Glasgow Coma Score <12/15 were included. Informed consent was obtained through a deferred-consent procedure.Intervention and comparator
A commercially available 1.4 mg/0.1 mL intranasal naloxone was compared with 0.8 mg/2 mL naloxone administered intramuscularly.Measurements
The primary end-point wa
SUBMITTER: Skulberg AK
PROVIDER: S-EPMC9302677 | biostudies-literature | 2022 Jun
REPOSITORIES: biostudies-literature