Clinical Trials Directory

Trials / Completed

CompletedNCT03649763

Onset and Duration of Forearm Nerve Blockade

Onset and Duration of Forearm Nerve Blockade Performed With a Single Distal Injection Versus Sequential Injections at Distal and Proximal Locations Alongside the Nerves: A Blinded Randomized

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
36 (actual)
Sponsor
New York School of Regional Anesthesia · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

This pilot study will evaluate the latency of onset and duration of sensory-motor block in patients undergoing hand surgery. Patients will be randomized to receive nerve blocks of the distal forearm or of the distal and proximal forearm. Local anesthetic will be injected to anesthetise the median and ulnar nerves in the distal forearm (1-injection site group) or the median and ulnar nerves in the distal and proximal forearm (2-sequential injection sites group) to accomplish anesthesia for surgery on the hand.

Conditions

Interventions

TypeNameDescription
DRUGLidocainelidocaine 1%, distal ( ulnar and medial nerve): 6ml/nerve , 12m total
DRUGBupivacaineBupivacaine 0.5%,distal ( ulnar and medial nerve): 6ml/nerve , 12m total
DRUGLidocainelidocaine 1%, distal and proximal ( ulnar and medial nerve): 3ml/nerve , 12m total

Timeline

Start date
2018-03-07
Primary completion
2018-12-31
Completion
2018-12-31
First posted
2018-08-28
Last updated
2019-02-26

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT03649763. Inclusion in this directory is not an endorsement.