Evaluation of the Change of Penile Corpus Cavernosum After Caudal Block Using Ultrasonography in Children
NCT ID: NCT02345785
Last Updated: 2019-02-26
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
6 participants
OBSERVATIONAL
2015-10-02
2016-01-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Group 1
pediatric patients who need urologic surgery and caudal block
urologic surgery and caudal block
Interventions
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urologic surgery and caudal block
Eligibility Criteria
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Inclusion Criteria
2. Children who needed caudal block for postoperative analgesia
Exclusion Criteria
2. patients scheduled for penile surgery
2 Years
7 Years
ALL
No
Sponsors
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Yonsei University
OTHER
Responsible Party
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Locations
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Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine
Seoul, , South Korea
Countries
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Other Identifiers
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4-2014-0891
Identifier Type: -
Identifier Source: org_study_id
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