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Clinical Trial Summary

There is an ongoing debate whether antihypertensive treatment with beta-blockers and/or angiotensin converting Enzyme (ACE)-inhibitors comprises a risk factor for more severe and more frequent side-effects during venom immunotherapy (VIT). In the literature, data are controversial and originate from case reports or statistically underpowered studies; the number of included patients was usually high but the proportion of patients on antihypertensive treatment was low ranging from 2-11%. The study was conducted as a prospective, observational, European multicenter study. 1425 patients, aged from 35 to 85 years, with a history of an anaphylactic reaction due to bee or wasp stings, were included. The medical history was recorded as well as laboratory parameters and data of the VIT-updosing phase. One year after reaching the maintenance dose, possible side-effects during VIT as well as the outcome of field stings or sting challenges were documented.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04269629
Study type Observational
Source Medical University of Graz
Contact
Status Completed
Phase
Start date August 2014
Completion date March 2019

See also
  Status Clinical Trial Phase
Active, not recruiting NCT00947908 - Regulation of Blood Dendritic Cells During Immune Therapy for Hymenoptera Venom Allergy N/A