Clinical Trials Directory

Trials / Completed

CompletedNCT02447497

In Vivo Patient Preoperative Skin Prep Persistence

Assessment of Antimicrobial Persistence of 3M CHG/IPA Preoperative Skin Preparation Against Resident Flora on the Abdominal and Inguinal Regions

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
27 (actual)
Sponsor
Solventum US LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

The objective of the study is to demonstrate persistence of the CHG/IPA Prep versus a saline placebo on skin flora of the abdominal and inguinal regions of human subjects as measured by change in microbial flora relative to baseline.

Conditions

Interventions

TypeNameDescription
DRUG3M CHG/IPA Surgical Skin Preparation - Abdominal RegionChlorhexidine gluconate 2% / Isopropyl alcohol 70%
OTHERNormal Saline - Abdominal Region0.9% sodium chloride applied with foam applicator
DRUG3M CHG/IPA Surgical Skin Preparation - Inguinal RegionChlorhexidine gluconate 2% / Isopropyl alcohol 70%
OTHERNormal Saline - Inguinal Region0.9% sodium chloride applied with foam applicator

Timeline

Start date
2015-03-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2015-05-19
Last updated
2024-10-02
Results posted
2020-11-23

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT02447497. Inclusion in this directory is not an endorsement.