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Randomized Trial of Intranasal Versus Intravenous Naloxone in Level of Consciousness in Suspected Opioid Overdose

This study has been completed.
Information provided by:
Isfahan University of Medical Sciences Identifier:
First received: February 9, 2011
Last updated: NA
Last verified: March 2007
History: No changes posted
The purpose of this study is to determine which route of administration is better for treatment of opioid overdosed patients

Condition Intervention Phase
Morphinan Opioid Overdose
Drug: Intranasal naloxone
Drug: Intravenous
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Study of Routs of Naloxone Administration for Opioid Overdosed Patients

Resource links provided by NLM:

Further study details as provided by Isfahan University of Medical Sciences:

Primary Outcome Measures:
  • level of consciousness [ Time Frame: 4 min after naloxone administration ]
    The investigators evaluated the level of consciousness with Glasgow coma sclae 4 minutes after naloxone administration

Secondary Outcome Measures:
  • blood pressure [ Time Frame: at 4 min after naloxone administration ]
    The investigators evaluated blood pressure 4 minutes after naloxone administration

Enrollment: 100
Study Start Date: March 2007
Study Completion Date: June 2007
Primary Completion Date: June 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
The investigators administered intravenous naloxone for our opioid overdose patients
Drug: Intravenous
Amp naloxone, 0.4 mg / each 4 minutes till increasing patient level of consciousness
The investigators administered intranasal naloxone for treatment of our patients
Drug: Intranasal naloxone
spray naloxone, 0.4 mg/ each 4 minutes till increasing patient level of consciousness

Detailed Description:
In intravenous drug abusers (IDUs), as a result of previous intravenous substance abuse, the predictable difficult cannulate exist and cause the delay administration of antidote therapy. Additionally, IDUs are also at increased risk of carrying blood borne infections that could be transmitted to healthcare workers through needle stick injuries. The investigators aimed to compare intranasal administration of naloxone with intravenous route.

Ages Eligible for Study:   15 Years to 50 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Patients with the range of 15-50 years old

    • Who were suspicious to opioid overdoses based on history and having clinical appearance such as miotic pupils with loss of consciousness
    • Give response to naloxone with increasing the level of consciousness

Exclusion Criteria:

  • Not giving response to naloxone and suspicious to have another reason for loss of consciousness
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Please refer to this study by its identifier: NCT01293058

Iran, Islamic Republic of
Noor university hospital
Isfahan, Iran, Islamic Republic of
Sponsors and Collaborators
Isfahan University of Medical Sciences
Principal Investigator: Nastaran Izadi, A.Professor Isfahan University of Medical Sciences
  More Information

Additional Information:
Responsible Party: Dr. Alireza Yousefy, Associate Professor of Medical Education, Isfahan University of Medical Sciences Identifier: NCT01293058     History of Changes
Other Study ID Numbers: ASD-1213-16
Study First Received: February 9, 2011
Last Updated: February 9, 2011

Keywords provided by Isfahan University of Medical Sciences:

Additional relevant MeSH terms:
Drug Overdose
Substance-Related Disorders
Chemically-Induced Disorders
Analgesics, Opioid
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents
Narcotic Antagonists processed this record on May 25, 2017