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Lidocaine and Ketamine Versus Standard Care on Acute and Chronic Pain

Study:

The Effect of Thoracolumbar Paravertebral Block or Intravenous Lidocaine and Ketamine Versus Standard Care on Acute and Chronic Pain After Inguinal Herniorrhaphy

Rationale:

n/a

Purpose:

The investigators are conducting this study to find out if intravenous (injected through the vein) infusion of lidocaine and ketamine administered with general anesthesia is as effective as a paravertebral block in lessening pain after surgery and that both of these techniques are superior to general anesthesia alone in reducing pain immediately after surgery and in the long-term.

Study Status: Terminated

Recruiting:
n/a

Condition Intervention Phase
Pain
Nausea
Drug: ropivacaine
Drug: Lidocaine/Ketamine
Other: placebo
N/A

Verified by Outcomes Research Consortium March, 2010

Sponsored by: Outcomes Research Consortium
Information provided by: Outcomes Research Consortium
ClinicalTrials.gov identifier: NCT00720330

Study Type: Interventional

Study Design: Allocation: Randomized, Control: Active Control, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Cleveland Clinic/Hillcrest Hospital
Mayfield Heights, Ohio 44124
United States

Kenneth Cummings, MD., Principal Investigator
Daniel I Sessler, MD., Study Chair

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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