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临床试验/NL-OMON39544
NL-OMON39544已完成3 期

A double blind randomized placebo controlled study on the efficacy of intralymphatic immunotherapy in the treatment of grasspollen induced allergic rhinitis. - ILIT

HagaZiekenhuis0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Sensibilisation to grass pollen
  • age between 18 and 50 years old
  • Informed consent

排除标准

  • No informed consent
  • instable or steroidtherapy dependent atopic astma
  • rhinosinusitis
  • nasal polyps
  • vasomotore rhinitis
  • immunosupressive medication
  • immuondeficiancy (IgG-IgA deficiaccy, HIV-AIDS)
  • pregnany or nursing
  • participation in other medical study
  • history of desensibilisation therapy
  • Significant cardiovascular disease
  • Severe impaired renal function
  • Hypersensitivity to aluminiumhydroxid
  • Childeren untill age of 18
  • Blood donation within previous 30 days
  • Surgery within the previous 30 days
  • Use of investigational drugs within previous 90 days
  • Mastocytosis
  • Hypertension
  • Active infectious disease
  • Significant hepatic disease
  • Significant renal disease
  • Significant hematological disorder
  • Significant pulmonary disease
  • Moderate or severe asthma
  • Autoimmune disease
  • History of malignancy.
  • Contraindicated medications were immunosuppressive agents, beta-blockers, ACE-inhibitors, and tricyclic antidepressants.

研究者

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