A Comparative Analysis of Prognostic Factors for Functional Outcomes in Patients With Acute Subdural Hematoma
NCT ID: NCT06364059
Last Updated: 2025-11-19
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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COMPLETED
175 participants
OBSERVATIONAL
2024-06-01
2025-11-04
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Surgery Group
Adult patients who underwent surgery due to acute subdural hematoma
Decompressive craniectomy with evacuation of subdural hematoma
Adult patients who underwent decompressive craniectomy with evacuation of subdural hematoma.
Interventions
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Decompressive craniectomy with evacuation of subdural hematoma
Adult patients who underwent decompressive craniectomy with evacuation of subdural hematoma.
Eligibility Criteria
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Inclusion Criteria
* 12 months of follow-up
* functional outcome measured by the Glasgow Outcome Scale Extended (GOSE).
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Military University Hospital, Prague
OTHER
Charles University, Czech Republic
OTHER
Responsible Party
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Michal Soták
Principal investigator
Principal Investigators
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Tomáš Tyll, M.D., Ph.D.
Role: STUDY_DIRECTOR
Charles University, Czech Republic
Locations
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Military University Hospital Prague
Prague, , Czechia
Countries
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Other Identifiers
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aSDH-TT
Identifier Type: -
Identifier Source: org_study_id
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