The acceptability, safety and tolerability of combined methadone-naloxone in methadone maintained individuals aged between 18 - 65
Phase 2
Completed
- Conditions
- Participants are opiod dependant and methadone maintained individuals aged between 18-65Mental Health - Addiction
- Registration Number
- ACTRN12608000024347
- Lead Sponsor
- angton Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
• Opioid dependent clients;
• In treatment for greater than 2months
• Stabilised on current dose for greater than 4 weeks
• Willing to remain on current dose for duration of the trial
• Venous access
• Able to provide voluntary informed consent
Exclusion Criteria
• Considered unwilling, unable or unlikely to comply with the study protocol
• Lactating and pregnant women
• Active psychotic illness
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method