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
76 participants
INTERVENTIONAL
2001-01-31
2006-02-28
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
PREVENTION
SINGLE
Study Groups
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regular bandage
no abdominal binder
no binder
abdominal binder
binder
abdominal binder
Interventions
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abdominal binder
no binder
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Brooke Army Medical Center
FED
Responsible Party
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Edward R. Kost, M.D.
Principal Investigator
Locations
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Brooke Army Medical Center
Fort Sam Houston, Texas, United States
Countries
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Other Identifiers
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C.2001.128
Identifier Type: -
Identifier Source: org_study_id
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