Clinical Trials Directory

Trials / Completed

CompletedNCT01112020

Components of Chlorhexidine Gluconate Dressing

Components & Tolerability of Chlorhexidine Gluconate Dressing Patch Compared to BioPatch & Tegaderm Chlorhexidine Gluconate Securement Dressing After Application to Healthy Subjects Over a 7-day Period

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
45 (actual)
Sponsor
C. R. Bard · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the contents of a chlorhexidine-containing dressing after use.

Detailed description

To characterize the chemical composition of the CHG (2% CHG) Catheter Dressing Patch as compared to Biopatch Protective Disk with CHG, and Tegaderm IV (intravenous) Securement Dressing over a wear period of 7 days.

Conditions

Interventions

TypeNameDescription
DEVICECHG Catheter Dressing Patch2% CHG dressing applied to 7 sites
DEVICEBiopatchBiopatch applied to 7 sites
DEVICETegaderm CHGTegaderm CHG IV Securement Dressing applied to 7 sites

Timeline

Start date
2010-04-01
Primary completion
2010-05-01
Completion
2010-05-01
First posted
2010-04-28
Last updated
2025-11-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01112020. Inclusion in this directory is not an endorsement.

Components of Chlorhexidine Gluconate Dressing (NCT01112020) · Clinical Trials Directory