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Clinical Trial Summary

The investigatoris will carefully select cartilage-hair hypoplasia patients unexposed to varicella (VZV) and immunize patients in a controlled manner with VZV vaccine. Patients will be selected on the basis of disease severity and the degree of immunodeficiency (including CD4+ T-cell counts). Any potential complication of VZV immunization, such as rash, will be discussed with the patients/caregivers beforehand and acyclovir will be used to treat any VZV related symptoms, consistent with the current practices. The investigators will verify the development of immune response to vaccination by testing for VZV antibodies and cell-mediated immunity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02383797
Study type Interventional
Source Helsinki University Central Hospital
Contact
Status Active, not recruiting
Phase Phase 4
Start date February 2015
Completion date February 2020