Prospective blinded randomised placebo controlled trial investigating whether oxycodone modified release reduces parenteral opioid use following intermediate thoracic surgery
Not Applicable
Completed
- Conditions
- Post-operative pain following intermediate thoracic surgerySurgeryPost-operative pain
- Registration Number
- ISRCTN14478115
- Lead Sponsor
- Harefield Hospital (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients scheduled for unilateral intermediate thoracic surgery (e.g. pleural abrasion, talc pleurodesis and lung biopsy)
Exclusion Criteria
Not provided at time of registration
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method