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Sedation During Microelectrode Recordings Before Deep Brain Stimulation for Movement Disorders.

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00355927
Enrollment
20
Registered
2006-07-25
Start date
2006-09-30
Completion date
2008-07-31
Last updated
2007-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dystonia, Movement Disorders, Parkinson Disease, Parkinsonian Disorders, Tourette Syndrome

Keywords

Deep brain stimulation, Microelectrode recordings, Basal Ganglia, Sedation, Propofol

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.

Interventions

PROCEDURESedation with IV propofol

Propofol(50 microgram/kg/min.), I.V. for 5-10 minutes, Until a level of light sedation is achieved

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Changes in the electrical activity of neuron cells of the basal ganglia in the examined patientsWithin 24 hours needed to analyse the data

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026