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Spinal Anesthesia With Articaine and Bupivacaine for Outpatient Lower Limb Surgery

NCT00332735 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2007-04-19

No results posted yet for this study

Summary

The purpose of the trial is to compare two local anesthetics, articaine and bupivacaine for outpatient lower limb surgery. Onset and recovery times of sensory and motor blockade will be compared.

Conditions

  • Spinal Anesthesia

Interventions

DRUG

spinal administration of articaine

DRUG

spinal administration of bupivacaine

Sponsors & Collaborators

  • Reinier de Graaf Groep

    lead OTHER

Principal Investigators

  • Tessa Dijkstra, drs · Reinier de Graaf Groep

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-05-31
Completion
2007-01-31

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 NCT00332735 on ClinicalTrials.gov