In Vivo Patient Preoperative Skin Prep Persistence
Completed · Phase 2
Conditions studied: Bacterial Recovery of Skin Flora Post-Product Application
In brief
The objective of the study is to demonstrate persistence of the CHG/IPA Prep on skin flora of the abdominal and inguinal regions of human subjects.
Key facts
- Study ID
- NCT02447497
- Run by
- Solventum US LLC
- People needed
- 27
- Starts
- 2015-03-01
- Expected to finish
- 2015-04-01
- Last updated by the study team
- 2024-10-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subjects of any race
- Subjects in good general health
- Minimum skin flora baseline requirements on abdomen and groin
You may not qualify if…
- Any tattoos, scars, breaks in the skin, or any form of dermatitis, or other skin disorders (including acne) on the applicable test areas
- Topical antimicrobial exposure within 14 days prior to screening and treatment days
- Use of systemic or topical antibiotics, steroid medications, or any other products known to affect the normal microbial flora of the skin within 14 days prior to screening and treatment days
Where it is running
- MicroBioTest — Sterling, Virginia, United States
Full record on ClinicalTrials.gov
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