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
| Type | Name | Description |
|---|---|---|
| DRUG | 3M CHG/IPA Surgical Skin Preparation - Abdominal Region | Chlorhexidine gluconate 2% / Isopropyl alcohol 70% |
| OTHER | Normal Saline - Abdominal Region | 0.9% sodium chloride applied with foam applicator |
| DRUG | 3M CHG/IPA Surgical Skin Preparation - Inguinal Region | Chlorhexidine gluconate 2% / Isopropyl alcohol 70% |
| OTHER | Normal Saline - Inguinal Region | 0.9% 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT02447497. Inclusion in this directory is not an endorsement.