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Clinical Trials/EUCTR2009-015867-15-IT
EUCTR2009-015867-15-IT
Active, not recruiting
Not Applicable

Different Anesthesiological Strategies Evaluation in Deep Brain Stimulation Neurosurgeries - DBS

AZIENDA OSPEDALIERA SAN GERARDO DI MONZA0 sitesFebruary 12, 2010
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ConditionsParkinson Desease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Desease
Sponsor
AZIENDA OSPEDALIERA SAN GERARDO DI MONZA
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 12, 2010
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
AZIENDA OSPEDALIERA SAN GERARDO DI MONZA

Eligibility Criteria

Inclusion Criteria

  • •\- Patients selected for elective neurosurgical interventions related to the implantation of intracranial electrodes deep. \- Good physical condition assessed in accordance with the general scale ASA (American Society of Anesthesiology, http://www.asahq.org/clinical/physicalstatus.htm) with classification I to III. \- Age between 18\-75 years. \- Normal preoperative supervision and safety for both the strategies Anesthetic (not contraindications for both).
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •\- Presence of severe cardiovascular disease (uncontrolled hypertension, lack of documented coronary reserve). \- The presence of liver or kidney disease that preclude the use of certain techniques anesthetic considered. \- Pregnancy. \- Known allergy to any form of anesthetic. \- Weight\> 120 Kg \- History of drug abuse or psychiatric disorders. \- Participation in other clinical studies over the past two months. \- Inability or refusal of informed consent in expression.

Outcomes

Primary Outcomes

Not specified

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