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Tracking Information | |||||||||||||
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First Received Date † | April 4, 2007 | ||||||||||||
Last Updated Date | April 4, 2007 | ||||||||||||
Start Date † | October 2006 | ||||||||||||
Current Primary Outcome Measures † | |||||||||||||
Original Primary Outcome Measures † | |||||||||||||
Change History | No Changes Posted | ||||||||||||
Current Secondary Outcome Measures † | |||||||||||||
Original Secondary Outcome Measures † | |||||||||||||
Descriptive Information | |||||||||||||
Brief Title † | The Utility of Performing Brain CT Scan in Non Trauma Patients at the Pediatric Emergency Unit | ||||||||||||
Official Title † | The Utility of Performing Brain CT Scan in Non Trauma Patients at the Pediatric Emergency Unit. A Retrospective Observational Study. | ||||||||||||
Brief Summary | Pediatric patients are admitted to the emergency room for diverse causes, beside trauma, patients can present with convulsions, suspicion of brain tumor or increased intracranial pressure. In most of the cases a brain CT is performed even before physical examination by a skilled neurologist. The amount of radiation that the children are exposed is equivalent to 100 plain chest X rays. The purpose of this tudy is to examinate in a retrospective study what were the indications for CT study and what was the incidence of relevant abnormal findings that required emergency intervention or referral. |
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Detailed Description | |||||||||||||
Study Phase | |||||||||||||
Study Type † | Observational | ||||||||||||
Study Design † | Natural History, Cross-Sectional, Defined Population, Retrospective Study | ||||||||||||
Condition † |
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Intervention † |
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Study Arms / Comparison Groups | |||||||||||||
Publications * | |||||||||||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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Recruitment Information | |||||||||||||
Recruitment Status † | Completed | ||||||||||||
Enrollment † | |||||||||||||
Completion Date | March 2007 | ||||||||||||
Primary Completion Date | |||||||||||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||||||||||
Ages | up to 18 Years | ||||||||||||
Accepts Healthy Volunteers | No | ||||||||||||
Contacts †† | |||||||||||||
Location Countries † | Israel | ||||||||||||
Expanded Access Status | |||||||||||||
Administrative Information | |||||||||||||
NCT ID † | NCT00456391 | ||||||||||||
Responsible Party | |||||||||||||
Secondary IDs †† | |||||||||||||
Study Sponsor † | HaEmek Medical Center, Israel | ||||||||||||
Collaborators †† | |||||||||||||
Investigators † |
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Information Provided By | HaEmek Medical Center, Israel | ||||||||||||
Verification Date | April 2007 | ||||||||||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |