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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UNKNOWN
50000 participants
OBSERVATIONAL
2005-01-31
Brief Summary
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Detailed Description
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Hospital based outpatient wound centers participating in the US Wound Registry agree to provide data as part of quality initiatives and to meet their Stage 2 Meaningful use criteria. The CTPR is a subset of the USWR data. All patient data from all participating outpatient clinics are transmitted to the USWR where it is available for benchmarking, PQRS and other initiatives. Data used for effectiveness research is HIPAA de-identified. These data are derived from structured language entries directly transmitted from electronic health records which also link to billing and charge documents once practitioners sign and lock charts, confirming the veracity of data entries.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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wounds treated with CTPs
All cellular and tissue based products currently reimbursed in the hospital based outpatient department, administered at intervals as determined in the course of clinical practice
Cellular and tissue based products
Procedure: Application of device or biological to wounds
Interventions
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Cellular and tissue based products
Procedure: Application of device or biological to wounds
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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U.S. Wound Registry
OTHER
Responsible Party
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Locations
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St. Luke's Wound Care Clinic
The Woodlands, Texas, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CDR002
Identifier Type: -
Identifier Source: org_study_id
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