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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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23 March 2015 |
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Main ID: |
NCT02385942 |
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Date of registration:
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03/03/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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KT(KT Corporation)-SNUBH(Seoul National University Bundang Hospital) U-health Cooperative Research
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Scientific title:
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KT-SNUBH U-health Cooperative Research: Target Selection and Consumers' Intention Research for Commercialization of the Pressure Ulcer Management u-Health Solution |
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Date of first enrolment:
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July 2012 |
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Target sample size:
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60 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT02385942 |
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Study type:
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Interventional |
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Study design:
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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Phase:
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N/A
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Countries of recruitment
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Korea, Republic of
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Contacts
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Name:
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Chanyeong Heo, Ph.D |
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Address:
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Telephone:
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Email:
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Affiliation:
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Seoul National University Bundang Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Subject who has pressure ulcer or Health care provider for wound management
Exclusion Criteria:
- Subject who have Osteomyelitis
- Subject who have suppuration
- Subject who participated in other clinical trial within 30 days from screening date
Age minimum:
21 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Pressure Ulcer
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Intervention(s)
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Device: Smart phone
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Primary Outcome(s)
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concordance rate of wound size between live assessed wound size and transmitted wound size
[Time Frame: a week from post treatment]
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Secondary Outcome(s)
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concordance rate of wound size between live assessed wound size and transmitted wound size
[Time Frame: 2 weeks from post treatment]
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concordance rate of wound size between live assessed wound size and transmitted wound size
[Time Frame: 3 weeks from post treatment]
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concordance rate of wound size between live assessed wound size and transmitted wound size
[Time Frame: 4 weeks from post treatment]
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Secondary ID(s)
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E-1206/158-001
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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