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Clinical Trials/NCT03174067
NCT03174067
Completed
Phase 4

Buprenorphine in the Emergency Department: Buprenorphine Versus Clonidine for Opioid Withdrawal

St. Joseph's Health Centre Toronto0 sites26 target enrollmentMarch 2013

Overview

Phase
Phase 4
Intervention
Buprenorphine
Conditions
Opioid Withdrawal
Sponsor
St. Joseph's Health Centre Toronto
Enrollment
26
Primary Endpoint
Number of participants attending the rapid access clinic
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This is a pilot randomized control trial randomizing patients presenting in opioid withdrawal to the emergency department to receive either one of clonidine (usual standard of care) or buprenorphine for their opioid withdrawal. Primary treatment outcome is attendance at a rapid access addiction medicine clinic within a few days of emergency room presentation. Secondary treatment outcome is treatment status with respect to opioid agonist treatment at one month post emergency room visit.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
November 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
St. Joseph's Health Centre Toronto
Responsible Party
Principal Investigator
Principal Investigator

Anita Srivastava

Staff Physician and Associate Professor

St. Joseph's Health Centre Toronto

Eligibility Criteria

Inclusion Criteria

  • Presenting to the ED in opioid withdrawal or soon to be in withdrawal
  • Minimum age 16
  • English speaking
  • Active phone number
  • Ontario Health Insurance Program card

Exclusion Criteria

  • Currently enrolled in a methadone or buprenorphine maintenance
  • Benzodiazepine addiction (or taking \>50mg of valium equivalent/day)
  • Acute hepatitis or liver failure

Arms & Interventions

Buprenorphine

Patient receives buprenorphine in the emergency room based on a clinical trial protocol as well as a take home prescription for buprenorphine

Intervention: Buprenorphine

Clonidine

Patient receives clonidine in the emergency room based on a clinical trial protocol and also receives a take home prescription for clonidine

Intervention: Clonidine

Outcomes

Primary Outcomes

Number of participants attending the rapid access clinic

Time Frame: 2-5 days

The number of participants who attend a rapid access clinic assessment after initial enrollment

Secondary Outcomes

  • Number of participants who are on opioid agonist treatment(30 days)

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