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Assessment of the Nociception During Lumbar Surgery

NCT01015651 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2010-04-07

No results posted yet for this study

Summary

The aim of the study is to assess the accuracy of a new paradigm in measuring the level of nociception during lumbar surgery. The paradigm is based the measurement of the baroreflex in response to noxious stimuli in anesthetized patients.

Conditions

  • Lumbar Surgery

Interventions

DRUG

remifentanil

anesthesia is induced and maintained with a target-controlled infusion of remifentanil at 2 ng/ml.

DRUG

remifentanil

anesthesia is induced and maintained with a target-controlled infusion of remifentanil at 4 ng/ml.

Sponsors & Collaborators

  • University Hospital, Grenoble

    lead OTHER

Principal Investigators

  • Jean-Francois PAYEN, M.D. · University Hospital, Grenoble

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2009-10-31
Completion
2009-10-31

Countries

  • France

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 NCT01015651 on ClinicalTrials.gov