Clinical Trials Directory

Trials / Completed

CompletedNCT00247741

Spinal Anesthesia With Articaine and Lidocaine for Outpatient Surgery.

Spinal Anesthesia With Articaine and Lidocaine for Outpatient Surgery: A Double Blind Randomized Clinical Trial.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
80 (planned)
Sponsor
St. Antonius Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare two short-acting local anesthetics, articaine and lidocaine, for spinal anesthesia in day-case surgery. The onset time of the sensory- and motor block, recovery time until discharge and complications will be studied.

Detailed description

The ideal spinal anesthesia in day-case surgery is characterized by a short onset of sensory and motor blockade, and a rapid recovery after the operation. Short-acting local-anesthetics are used frequently in this setting. Lidocaine is one of the agents that is used most frequently. It has been associated with an increased incidence of Transient Neurological Symptoms (TNS). Articaine is another agent that is being used more often and is said to act faster and shorter than lidocaine. We will compare spinal anesthesia with lidocaine and articaine in a randomized double-blind clinical trial. Endpoint are: * onset of sensory and motor block * recovery from sensory and motor block * time to micturition * patient satisfaction * complications

Conditions

Interventions

TypeNameDescription
DRUGspinal administration of articaine
DRUGspinal administration of lidocaine

Timeline

Start date
2005-11-01
Completion
2006-05-01
First posted
2005-11-02
Last updated
2013-12-19

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00247741. Inclusion in this directory is not an endorsement.