Randomised controlled trial of port wound and intrapleural bupivacaine analgesis versus saline
Not Applicable
Completed
- Conditions
- SurgeryAnaesthesiaSurgery: Anaesthesia
- Registration Number
- ISRCTN88537312
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2006 Update - Department of Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Not provided at time of registration
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
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie bupivacaine's analgesic effects in port wound and intrapleural administration for postoperative pain?
How does port wound and intrapleural bupivacaine analgesia compare to standard opioid-based postoperative pain management in surgical patients?
Which biomarkers correlate with improved pain outcomes in bupivacaine versus saline analgesia trials for thoracic surgery?
What are the safety profiles and management strategies for intrapleural bupivacaine administration in ISRCTN88537312?
What combination therapies or alternative analgesics have been evaluated alongside bupivacaine for enhanced postoperative pain relief in surgical contexts?