urticartia, urticaria factitia, dermographic urticaria, netelroos
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: General inclusion criteria In order to be eligible to participate in this study, a subject must meet all of the following criteria: - 18 years or older - Informed consent given Inclusion criteria for UF patients In order to be eligible to participate in this study, a UF patient must meet all of the following criteria: - UF diagnosed by a dermatologist - UF in active phase, i.e., wheals arise when antihistaminic drugs are stopped
Exclusion criteria
Exclusion criteria: General exclusion criteria A potential subject who meets any of the following criteria will be excluded from participation in this study: - Participants that cannot read, speak or understand Dutch - Mentally incompetent individuals who are not capable to provide informed consent, as determined by their treating physician - Conditions that will cause excessive MEG artefacts (cardiac pacemaker/cardiac or neural defibrillators, metal fragments in the eyes, metal plates, piercings, pins or bolts in head, any magnetic implantation/implantations made from iron (ferrous products, including braces and splints) - Systemic medication: corticosteroids, ciclosporine, montelukast, hydroxychloroquine, dapson, omalizumab, methotrexate - The antihistaminic drug should be stopped 4 days in advance Exclusion criteria for healthy controls - Participants with a history of any form of urticaria - Participants who use antihistaminic drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Difference in local and global connectivity between UF patients and healthy controls during the baseline measurement - Difference in local and global connectivity between UF patients and healthy controls after a histamine prick test - Difference in local and global connectivity between UF patients and healthy controls after dermography | — |
Secondary
| Measure | Time frame |
|---|---|
| - Differences in the itch score (VAS) before and after a histamine prick test and dermography, DASS and serum levels of stress related mediators (CRH, ACTH, prolactine, cortisol, NGF, BDNF, SP) between UF patients and the control group. - Correlation between ‘global connectivity’ after a histamine prick test and the itch score (VAS), area of a histamine prick test wheal and flare, UCT, CU-Q2oL, DASS and serum levels of stress mediators (CRH, ACTH, prolactine, cortisol, NGF, BDNF, SP). - Correlation between ‘global connectivity’ after dermography and the itch score (VAS), width of the dermography wheal, UCT, CU-Q2oL, DASS and serum levels of stress mediators (CRH, ACTH, prolactine, cortisol, NGF, BDNF, SP) In case of detectable regional differences in connectivity measures after a histamine prick test or dermography between UF patients and the control group: - Correlation between ‘local connectivity’ after a histamine prick test and the itch score (VAS), area of a histamine prick test wheal and flare, UCT, CU-Q2oL, DASS and serum levels of stress mediators (CRH, ACTH, prolactine, cortisol, NGF, BDNF, SP). - Correlation between ‘local connectivity’ after dermography and the itch score (VAS), width of the dermography wheal, UCT, CU-Q2oL, DASS and serum levels of stress mediators (CRH, ACTH, prolactine, cortisol, NGF, BDNF, SP). | — |