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
| Type | Name | Description |
|---|---|---|
| DEVICE | CHG Catheter Dressing Patch | 2% CHG dressing applied to 7 sites |
| DEVICE | Biopatch | Biopatch applied to 7 sites |
| DEVICE | Tegaderm CHG | Tegaderm 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.