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Spinal Anesthesia With Articaine and Lidocaine for Outpatient Surgery.

NCT00247741 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2013-12-19

No results posted yet for this study

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.

Conditions

  • Spinal Anesthesia

Interventions

DRUG

spinal administration of articaine

DRUG

spinal administration of lidocaine

Sponsors & Collaborators

  • St. Antonius Hospital

    lead OTHER

Principal Investigators

  • Leon Timmerman, MD · St Antonius Hospital, dept. of anesthesiology

  • Emile MJ Andriessen, MD · St Antonius Hospital, dept of anesthesiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-11-30
Completion
2006-05-31

Countries

  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00247741 on ClinicalTrials.gov