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
213 participants
OBSERVATIONAL
2010-12-31
2025-01-13
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Baylor Research Institute
OTHER
Responsible Party
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Principal Investigators
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Bernard Fischbach, MD
Role: PRINCIPAL_INVESTIGATOR
Baylor All Saints
Locations
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Baylor All Saint's Medical Center in Fort Worth
Fort Worth, Texas, United States
Countries
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Other Identifiers
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010-263
Identifier Type: -
Identifier Source: org_study_id
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