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Neuraxial Pethidine After Lumbar Surgery Trial

This study is currently Recruiting

January 2009 By Austin Health

First Recieved on September 9, 2005

Last Updated on January 29, 2009

Sponsor: Austin Health
Collaborators:
Information provided by: Austin Health
Identifier: NCT00163553

Purpose

The hypothesis is that epidural pethidine is an effective form of pain relief following lumbar spinal surgery, resulting in significantly lower usage of concomitantly administered (intravenous) patient-controlled analgesia (PCA) pethidine.

Study Type: Interventional
Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Eligibility

Ages Eligible for Study:18 Years
Genders Eligible for Study:Both
Accepts Healthy Volunteers:No
Criteria

Inclusion Criteria: - Adults undergoing lumbar spinal surgery Exclusion Criteria: - Lack of informed patient consent - Acute or chronic renal failure - Known allergy or intolerance to pethidine or tramadol - Chronic respiratory insufficiency - Epidural contraindicated (coagulopathy, systemic infection)

Investigators

  • Investigator: Dean A Cowie, MBBS, FANZCA - Principal Investigator - Austin Health

Locations

  • Austin Health

    Melbourne, Victoria 3084 Australia

Conditions related to this trial:

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