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Clinical Trials/ACTRN12611000852954
ACTRN12611000852954
Completed
Phase 2

Randomised, double-blinded clinical trial comparing intranasal and intramuscular naloxone for reversal of suspected opioid overdose in clients of the Sydney Medically Supervised Injecting Centre

Sydney Medically Supervised Injecting Centre0 sites200 target enrollmentAugust 10, 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Suspected acute opioid overdose
Sponsor
Sydney Medically Supervised Injecting Centre
Enrollment
200
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 10, 2011
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Sydney Medically Supervised Injecting Centre

Eligibility Criteria

Inclusion Criteria

  • All clients with symptoms/signs of an opioid overdose requiring Naloxone administration will be eligible for entry. This is based on existing and approved MSIC protocols and clinical criteria for overdose (reduced level of consciousness as measured by the Glasgow Coma Score, pinpoint pupils, respiratory depression and/or reduced oxygen saturations as measured by pulse oximetry).

Exclusion Criteria

  • Less than 18 years of age
  • Pregnant or suspected of being pregnant

Outcomes

Primary Outcomes

Not specified

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