Clinical Trials Directory

Trials / Completed

CompletedNCT03797235

The Impact of Nerve Cross Section Area on Sensory Block Onset

The Impact of Nerve Cross Section Area on Sensory Block Onset. A Prospective, Monocentric Crossover Study on Volunteers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Jose Aguirre · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Accepted

Summary

The study aims to describe a correlation between the nerve cross section and the sensory or motor block onset time. Therefore, different nerve cross sections with their Motor and sensory onset times are compared in order to find a correlation. In the case of discovering a correlation, this could be translated into clinical practice, where a more tailored and individualized approach to performing peripheral nerve blocks would be possible, thus lowering the risks of adverse events occurring.

Conditions

Interventions

TypeNameDescription
PROCEDUREDominant ArmThe volume of local anesthetic used for the block of the ulnar and median nerve will be 5 times the estimated 95% effective dose (ED 95 ) of LA needed to block the nerve relative to the nerve cross-sectional area. The ED 95 for the ulnar nerve has been elucidated to be 0,11ml/mm2. The same ED 95 will be used for the median nerve.
PROCEDURENon-dominant armThe volume of local anesthetic used for the block of the ulnar and median nerve will be 5 times the estimated 95% effective dose (ED 95 ) of LA needed to block the nerve relative to the nerve cross-sectional area. The ED 95 for the ulnar nerve has been elucidated to be 0,11ml/mm2. The same ED 95 will be used for the median nerve.

Timeline

Start date
2019-01-19
Primary completion
2019-06-20
Completion
2019-06-21
First posted
2019-01-09
Last updated
2020-05-22

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03797235. Inclusion in this directory is not an endorsement.