Acquisition of clinical parameter, time response data and body core temperature during active or passive warming and during the day of patients sufferring from cholinergic urticaria
- Conditions
- L50.5Cholinergic urticaria
- Registration Number
- DRKS00004277
- Lead Sponsor
- Charité Campus Charité Mitte
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 52
Inclusion Criteria
Volonteers (male or female), between 18 and 70 years od age, smoker or non smoker, valid healthy insurance, written informed consent, suspected to suffer from cholinergic urticaria
Exclusion Criteria
no valid health insurance, participation in another running study, Patients suffering from other diseases, that prohibt study participation (e.g. allergy against sensor material)
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Detection of the change in body core temperature with the double sensor that is needed to induce skin reaktions in the patients
- Secondary Outcome Measures
Name Time Method Detection of the change in body core temperature with the double sensor that is needed to induce skin reaktions in the patients