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
NA
337 participants
INTERVENTIONAL
2012-11-30
2014-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Interventions
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Computed Tomography scan
Routine Computed Tomography scan
Eligibility Criteria
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Inclusion Criteria
2. Subjects with relative clinical findings indicative for CT examination. CT referral request approved by a physician is needed
3. Voluntary signed the Informed Consent Form
Exclusion Criteria
2. Subjects who are not able or not willing to give written Informed Consent without a caregiver consent
ALL
No
Sponsors
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Philips Healthcare
INDUSTRY
Responsible Party
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Principal Investigators
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Jacob Sosna, MD
Role: PRINCIPAL_INVESTIGATOR
Locations
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Hadassah-Hebrew University Medical Center
Jerusalem, , Israel
Countries
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Other Identifiers
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iCT DL
Identifier Type: -
Identifier Source: org_study_id