Trials / Completed
CompletedNCT02157090
Clinical Assessment of the Effectiveness and Safety of Herpes Patch SOS in the Treatment of Herpes Simplex Labialis in Comparison to a Competitor's Product.
Clinical Assessment of the Effectiveness and Safety of Herpes Patch SOS (Hansaplast®) Based on Hydrocolloids Without Active Substances in the Treatment of Herpes Simplex Labialis in Comparison to a Competitor's Product (Herpes Vesicle Patch of COMPEED®)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- —
- Sponsor
- Technische Universität Dresden · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Recent clinical studies showed, that a hydrocolloid patch is effective, well tolerated and comparable with aciclovir cream 5 % for the treatment of HSL lesions, while affording additional benefits of wound protection, discretion and relief of social embarrassment. The aim of the actual study was the clinical assessment of the effectiveness and safety of Hansaplast® SOS Herpes Patch (HPHP) in comparison to Compeed® Herpes Vesicle Patch (CHP) in treating HSL. Both products are CE-certificated and are available at the market for medical devices.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Herpes Patch SOS (Hansaplast®) | |
| OTHER | Herpes vesicle patch of Compeed® |
Timeline
- Start date
- 2009-08-01
- Primary completion
- 2010-01-01
- Completion
- 2010-06-01
- First posted
- 2014-06-05
- Last updated
- 2014-06-05
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT02157090. Inclusion in this directory is not an endorsement.