Trials / Terminated
TerminatedNCT03369756
Prontosan Quality of Life Study in Patients With Chronic Leg Wound(s)
A Prospective Study of Quality of Life in Patients With Chronic Leg Wound(s) Treated With Prontosan® Wound Irrigation Solution and Prontosan® Wound Gel
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 43 (actual)
- Sponsor
- B. Braun Medical Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study evaluates the use of Prontosan® Wound Irrigation Solution and Prontosan® Wound Gel in the treatment of chronic leg wounds in adults. All participants will use Prontosan and report their personal observations regarding Quality of Life.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Prontosan Wound Irrigation Solution and Prontosan Wound Gel | Wound cleansing using Prontosan solution and gel |
Timeline
- Start date
- 2018-02-20
- Primary completion
- 2019-09-25
- Completion
- 2019-09-25
- First posted
- 2017-12-12
- Last updated
- 2020-12-08
- Results posted
- 2020-12-08
Locations
5 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03369756. Inclusion in this directory is not an endorsement.