Improving Informed Consent Process for Percutaneous Cholecystostomy in the Emergency Department
NCT ID: NCT01476319
Last Updated: 2017-04-07
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
22 participants
INTERVENTIONAL
2009-11-09
2014-09-09
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
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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control
No interventions assigned to this group
video
video
The intervention group includes patients who obtain information about percutaneous cholecystostomy from a video will view at their bedside on a laptop.
Interventions
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video
The intervention group includes patients who obtain information about percutaneous cholecystostomy from a video will view at their bedside on a laptop.
Eligibility Criteria
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Inclusion Criteria
* scheduled to receive the percutaneous cholecystostomy
Exclusion Criteria
* refuse to participate
* are unable to understand the study process
18 Years
ALL
No
Sponsors
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Kaohsiung Medical University Chung-Ho Memorial Hospital
OTHER
Responsible Party
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Yen-Ko Lin
Attending Physician
Locations
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Kaohsiung Medical University Chung-Ho Memorial Hospital
Kaohsiung, Taiwan, Taiwan
Countries
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Other Identifiers
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KMUH-IRB-980360
Identifier Type: -
Identifier Source: org_study_id
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