Clinical Trials Logo

Clinical Trial Summary

To investigate if the use of perioperative neuraxial blockade reduces post-operative mortality and cardiorespiratory events compared to intraoperative general anesthesia AND postoperative IV narcotic analgesia. This is a feasibility study to determine if recruitment and execution of the protocol could be done in a timely manner in a much larger trial


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00221260
Study type Interventional
Source University of British Columbia
Contact
Status Completed
Phase N/A
Start date September 2005
Completion date January 2008

See also
  Status Clinical Trial Phase
Terminated NCT02744352 - Single Shot vs Catheter Infraclavicular Brachial Plexus Block After Distal Radius Fracture Repair N/A
Withdrawn NCT02160301 - Effect of a Multimodal Pain Regimen on Pain Control, Patient Satisfaction and Narcotic Use in Orthopaedic Trauma Patients Phase 4
Completed NCT02730728 - Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA N/A
Terminated NCT03435692 - Post Operative Pain Control After Pediatric Hip Surgery N/A
Withdrawn NCT04444830 - Sprix for Postoperative Pain Control Following Gynecologic Surgery Phase 4
Completed NCT03250494 - Duloxetine and Dexamethasone for Improving Postoperative Pain Phase 4
Completed NCT03743194 - Pectoralis and Serratus Muscle Blocks Phase 4