A Feasibility Study to Evaluate Skin Cleansing With a Sodium Hypochlorite Wash
NCT ID: NCT03534388
Last Updated: 2019-09-25
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WITHDRAWN
NA
INTERVENTIONAL
2018-05-10
2019-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Prospective Subjects
Sodium Hypochlorite Cleanser
Cleansing with CLn BodyWash
Interventions
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Sodium Hypochlorite Cleanser
Cleansing with CLn BodyWash
Eligibility Criteria
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Inclusion Criteria
2. Subject is willing and able to give written informed consent and to comply with the requirements of the study.
3. Subject has 5 or more days of time prior to elective surgery scheduled to sign consent and begin washing parameters.
4. Subject is capable of taking a shower and lathering their entire body, or is able to be helped by a caregiver to shower each day with lather on their entire body for 5 out of 7 days immediately prior to elective surgery. (Modifications for bath usage can be made by the physician if the result of the product being left on the skin of the entire body for the time commitment is maintained, and if the body can be rinsed with poured water. Bed bath is not considered an allowable modification.)
Exclusion Criteria
2\) Subject is unable to maintain washing regimen for the full study term.
3\) Subject is unable to follow pre-surgery cleansing instructions for 5 of the 7 days immediately prior to surgery. (Bed bath is not considered a cleansing day.)
18 Years
ALL
No
Sponsors
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TopMD Skin Care, Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Stephen E Hohmann, MD
Role: PRINCIPAL_INVESTIGATOR
Texas Vascular Associates
Locations
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Texas Vascular Associates, PA
Dallas, Texas, United States
Countries
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Other Identifiers
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CLN 004.2
Identifier Type: -
Identifier Source: org_study_id
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