Chlorhexidine dressing patch tested on healthy volunteers – no health benefit expected
NCT ID NCT01112020
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed Phase 1 study tested how much chlorhexidine gluconate (CHG) and a breakdown product called PCA remain in different dressing patches after 7 days on healthy volunteers. 45 participants had patches applied to 7 sites each. The study was not designed to treat or prevent any disease, but to understand the dressing's contents after use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Chlorhexidine gluconate dressing patch
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
45 people
The number who actually took part.
- Start date
-
Apr 2010
- Finished
-
May 2010
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Able to read, review and sign the Informed Consent * Willing to shower using the same soap/cleansers from the Screening Visit through the end of the study * Use study-approved contraceptive methods Exclusion Criteria: * Participation in an investigational study within 28 days prior to dosing. * Clinically significant illness within 28 days prior to dosing. * History of allergic responses to chlorhexidine, chlorhexidine-containing products, glycerol, adhesives, latex * History of clinically significant skin disorders * History of Type I diabetes mellitus, insulin-dependent diabetes mellitus(IDDM) * History of significant dermatologic cancers (melanoma, squamous) * Known history of immunologic disorders * Use immunosuppressive or other proscribed medications * Use of skin products at the application site * Significant history of allergies to soaps, lotions, emollients, ointments, creams * History of drug or alcohol addiction within the past year * Pregnant, lactating, breast-feeding, or intends to become pregnant during the course of the study
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Cetero Research
Saint Charles, Missouri, 63301, United States
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