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
| Type | Name | Description |
|---|---|---|
| DRUG | spinal administration of articaine | |
| DRUG | spinal 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.