Clinical Trials Logo

Clinical Trial Summary

The "Shamrock method" is a new ultrasound-guided lumbar plexus block. The aim of the study is to determine the minimum effective volume of ropivacaine 0.5% required to produce an effective lumbar plexus block with this method. Using the Dixon and Massey up-and-down method study design, 30 patients scheduled for elective total hip and knee arthroplasty will be included in the study.


Clinical Trial Description

n/a


Study Design

Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor)


Related Conditions & MeSH terms

  • Mininimum Effective Anaesthetic Volume of Local Anaesthetic

NCT number NCT01956617
Study type Interventional
Source Oslo University Hospital
Contact
Status Completed
Phase N/A
Start date October 2013