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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WITHDRAWN
OBSERVATIONAL
2013-04-30
2018-04-01
Brief Summary
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After providing informed consent, participants will be asked a series of questions related to their past medical history, and relevant wound data will be collected. Study staff will photograph the wound at baseline, and once per week until the wound is completely healed, or for a duration of six months.
Participants will be expected to return to Winthrop University Hospital for wound follow-up on a regular basis, or as determined by the Principal Investigator.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Diagnosed with a wound (defined as a break in the integument)
* Must be willing and able to provide written informed consent
Exclusion Criteria
21 Years
ALL
No
Sponsors
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Winthrop University Hospital
OTHER
Responsible Party
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Principal Investigators
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Harold Brem, MD
Role: PRINCIPAL_INVESTIGATOR
Winthrop University Hospital
Locations
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Winthrop University Hospital
Mineola, New York, United States
Countries
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Related Links
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Related Info
Other Identifiers
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13308-1
Identifier Type: -
Identifier Source: org_study_id
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