Components of Chlorhexidine Gluconate Dressing
Completed · Phase 1
Conditions studied: Healthy
In brief
The purpose of this study is to determine the contents of a chlorhexidine-containing dressing after use.
Key facts
- Study ID
- NCT01112020
- Run by
- C. R. Bard
- People needed
- 45
- Starts
- 2010-04-01
- Expected to finish
- 2010-05-01
- Last updated by the study team
- 2025-11-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Cetero Research — Saint Charles, Missouri, United States
Full record on ClinicalTrials.gov
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