Clinical Trials Directory

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

TypeNameDescription
OTHERHerpes Patch SOS (Hansaplast®)
OTHERHerpes 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.