Phase
Condition
Lyme Disease
Rash
Treatment
N/AClinical Study ID
Ages 1-17 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
signed informed general consent
residence in cantons Basel city, Basel country, Aargau, Solothurn and neighboringareas of France and Germany (Germany postal codes 794x, 795x, 796x, 797x and Francepostal codes 68480, 68640, 68220, 68330, 68300, 68128, 68730, 68870, 68510, 68130, 68640, 68960, 56890, 68118, 68580, 68680, 68440, 68720)
Exclusion
Exclusion Criteria:
- case blood is taken repetitively from the same child, only the first sample will beused and the child will only be included in the study once.
Refugees seeking asylum will be excluded. These children will be identified by postal address of the Bundesasylzentrum.
Children presenting for a diagnosis related to a B. burgdorferi infection will beexcluded since including these children would result in an over-estimation of thepre-test prevalence of B. burgdorferi IgG due to a possible selection bias.Diagnosis related to a B. burgdorferi infection will include erythema migrans,borrelial lymphocytoma, early or late neuroborreliosis, acute arthritis or carditis,acrodermatitis chronica atrophicans.
Children with underlying chronic disease, that potentially affects plasma antibodieswill be excluded, these include for example the following conditions:
known inborn or acquired immunodeficiency syndrome
Systemic lupus erythematosus
Children with history of intravenous immunoglobulin treatment in the past 12months for any reason including Kawasaki Disease, Paediatric InflammatoryMultisystem Syndrome, Immunothrombocytopenia.
Children after allogenic stem cell transplantation.
Children with cancer or known chronic hematology disease.
Children treated with immunosuppressive treatment in the last 6 monthsincluding systemic steroids >2 weeks duration (>2mg/kg or >20 mg prednisoneequivalent) or immunosuppressive combination treatments (e.g. biologicaldisease modifying antirheumatic drugs (DMARDs) + conventional DMARDs),Rituximab or leflunomide
Study Design
Study Description
Connect with a study center
University Childrens Hospital Basel
Basel, 4031
SwitzerlandSite Not Available
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