Studies on healthy volunteers for basic experimental research purposes
Conditions
Interventions
Group 1: Two qutenza-patches 1.5x1.5cm (179mg capsaicin / 280cm²) with a distance of 1 cm in between and one placebo-patch 1.5x1.5cm at a distance of 5 cm from either qutenza-patch. Duration of applic
Sponsors
Experimentelle Schmerzforschung MCTN der Medizinischen Fakultät Mannheim der Universität Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: healthy
Exclusion criteria
Exclusion criteria: intake of anti-histaminergic medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endpoint: Changes in intensity of evoked sensation and skin reddening. Time point of assessment: immediately prior patch-application (d0), during patch administration at day1 and day4 (d1 and d4), weekly after patch removal for 12 weeks (d7-d14-d21-d28-d35-d42-d49-d56-d63-d70-d77-d84). | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in intensity of histamine-mediated itch (d4-d7-d14-d21-d28-d35-d42-d49-d56-d63-d70-d77-d84). | — |
Countries
Germany
Contacts
Public ContactRoman Rukwied
Experimentelle Schmerzforschung MCTN der Medizinischen Fakultät Mannheim der Universität Heidelberg
Outcome results
None listed