Clinical Trials Directory

Trials / Completed

CompletedNCT03310047

Intra-individual Reproducibility in Nerve Block Duration

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Nordsjaellands Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

An interventional randomized controlled crossover trial, to illuminate if durations in nerve block durations are predictable within the same subject.

Detailed description

An interventional randomized controlled crossover trial, with the purpose to elucidate the reproducibility in nerve block duration on 20 healthy volunteers in Denmark. There will be two trial arms: 1: Day one; Right side low dose nerve block and left side high dose nerve block. Repeated after 24 hours. Day three; Left side low dose nerve block and right side high dose nerve block. Repeated after 24 hours 2: Day one; Left side low dose nerve block and right side high dose nerve block Repeated after 24 hours Day three; Right side low dose nerve block and left side high dose nerve block Repeated after 24 hours All volunteers will receive two peripheral nerve blocking catheters adjacent to the common peroneal nerve and will be treated two times on each side with Lidocaine 0.5% 5 mL and 10 mL.

Conditions

Interventions

TypeNameDescription
DRUGInfusion, Lidocaine, 0.5%, 5 mLA catheter-based perineural infusion of 5 mL Lidocaine 0.5%
DRUGInfusion, Lidocaine, 0.5%, 10 mLA catheter-based perineural infusion of 10 mL Lidocaine 0.5%

Timeline

Start date
2017-10-30
Primary completion
2018-03-01
Completion
2018-03-01
First posted
2017-10-16
Last updated
2018-05-15

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT03310047. Inclusion in this directory is not an endorsement.