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Clinical Trials/NCT00355927
NCT00355927
Unknown
N/A

Changes of the Neuronal Activity in the Subthalamic Nucleus Under Propofol Sedation During Stereotactic Electrode Implantation.

Hadassah Medical Organization1 site in 1 country20 target enrollmentSeptember 2006

Overview

Phase
N/A
Intervention
Not specified
Conditions
Movement Disorders
Sponsor
Hadassah Medical Organization
Enrollment
20
Locations
1
Primary Endpoint
Changes in the electrical activity of neuron cells of the basal ganglia in the examined patients
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to detect possible changes in the electrical activity of the Basal Ganglia related to sedation during deep brain stimulation surgery.

Detailed Description

Deep Brain Stimulation is commonly used for the treatment of movement disorders. Electrode positioning is usually performed under local anesthesia in fully awake patients. The procedure is uncomfortable to the patients who have to remain motionless during the whole surgery. Previous reports of electrode positioning under general anesthesia was found to be less accurate. This result was probably due to the effect of the anesthetics on the electrical activity of the Basal Ganglia. The purpose of this study is to detect possible changes in the electrical activity of the Basal Ganglia related to propofol sedation. Electrical activity of single neurons will be recorded before and after sedation.

Registry
clinicaltrials.gov
Start Date
September 2006
End Date
July 2008
Last Updated
18 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Candidate for Deep Brain Stimulation Surgery.
  • Informed concent obtained.

Exclusion Criteria

  • Suspected difficult intubation (by history or physical examination).
  • Allergy to Propofol, eggs or soy-beans.
  • History of sleep apnea syndrome.

Outcomes

Primary Outcomes

Changes in the electrical activity of neuron cells of the basal ganglia in the examined patients

Time Frame: Within 24 hours needed to analyse the data

Study Sites (1)

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