Efficacy Study of Patient Preoperative Preps In-vivo

Completed · Phase 3

Conditions studied: Surgical Skin Preparation

In brief

The purpose of this study is to determine the antimicrobial efficacy of an investigational CHG/IPA prep on skin flora of the inguinal regions of human subjects.

Key facts

Study ID

NCT04756154

Run by

Solventum US LLC

People needed

154

Starts

2020-07-06

Expected to finish

2021-04-28

Last updated by the study team

2024-10-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects of any race
• Subjects in good health
• Minimum skin flora baseline requirements on inguinal region

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 area
• 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

• Microbac Laboratories, Inc — Sterling, Virginia, United States

Full record on ClinicalTrials.gov

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