The Neuroprotection of Sevoflurane Preconditioning on Intracranial Aneurysm Surgery
NCT ID: NCT01204268
Last Updated: 2010-09-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
80 participants
INTERVENTIONAL
2009-08-31
2011-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Propofol group
Patients will receive the total intravenous anesthesia with propofol infusion during the surgery.
No interventions assigned to this group
Sevo-C group
Patients will receive the anesthesia with continuous inhalation of sevoflurane.
Sevo continuous inhalation
Patients will receive the anesthesia with continuous inhalation of sevoflurane.
Sevo-I group
Sevoflurane will be given before the cerebral artery clip as a preconditioning procedure for the coming ischemia-reperfusion injury.
Sev-I group
Sevoflurane will be given before the cerebral artery clip as a preconditioning procedure for the coming ischemia-reperfusion injury.
Interventions
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Sev-I group
Sevoflurane will be given before the cerebral artery clip as a preconditioning procedure for the coming ischemia-reperfusion injury.
Sevo continuous inhalation
Patients will receive the anesthesia with continuous inhalation of sevoflurane.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
70 Years
ALL
No
Sponsors
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Xijing Hospital
OTHER
Responsible Party
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Xijing Hospital, Fourth Military Medical University
Principal Investigators
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Hailong Dong, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Xijing Hospital
Locations
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Xijing Hospital
Xi'an, Shaanxi, China
Countries
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Facility Contacts
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Other Identifiers
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APC-BRAIN-2009
Identifier Type: -
Identifier Source: org_study_id