Targin® for Chronic Pain Management in Patients With Spinal Cord Injury
NCT03179475 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1
Last updated 2021-12-10
Summary
The study will be investigating the effectiveness of oxycodone-naloxone (brand name Targin®) at treating chronic pain in individuals with spinal cord injury. The goal of the study is to compare the effectiveness of Targin® at treating chronic pain in individuals with sub-acute and chronic spinal cord injury compared to opioid medication that is not compounded with naloxone.
Conditions
Interventions
- DRUG
-
Oxycodone Naloxone Combination
A flexible dosing schedule will be used in this study. The dose and schedule will be based on the minimal amount of medication required to manage pain related to spinal cord injury. The dose and/or frequency will be titrated to the individual's pain level at the discretion of their regular attending physician and/or investigator. Oxycodone-Naloxone is available in the following oral dosages: 1. 5 mg oxycodone hydrocholoride / 2.5 mg naloxone hydrochloride 2. 10 mg oxycodone hydrocholoride / 5 mg naloxone hydrochloride 3. 20 mg oxycodone hydrocholoride / 10 mg naloxone hydrochloride 4. 40 mg oxycodone hydrocholoride / 20 mg naloxone hydrochloride
Sponsors & Collaborators
-
Purdue Pharma, Canada
collaborator INDUSTRY -
International Collaboration on Repair Discoveries
collaborator OTHER -
Vancouver Coastal Health
collaborator OTHER_GOV -
University of British Columbia
lead OTHER
Principal Investigators
-
Andrei Krassioukov, MD,PhD,FRCPC · University of British Columbia
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-09-05
- Primary Completion
- 2021-11-29
- Completion
- 2021-11-29
Countries
- Canada
Study Locations
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