EUCTR2007-004590-25-AT进行中（未招募）不适用
Determination of immune response after sequential pneumococcal vaccination using the 7-valent conjugate pneumococcal and the 23-valent pneumococcal polysaccharide vaccine in renal transplant recipients
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Adult patients will be recruited at the transplant center of the Medical University of Vienna.
- •Patients will be eligable if between 6 months and 3 years had passed since their kidney transplant and if they have stable allograft function, as evidenced by creatinine level < 250 µl for 1 month prior involvement
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •splenectomy, pneumococcal vaccination within preceeding 5 years, any acute febrile illness in the 2 weeks prior to or at time of enrollment, use of intravenous immunoglobulis within precceding 6 months, history of severe allergic reaction or anaphylaxis, hemoglobin value < 10 g/dl at the time of inclusion
研究者
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Evaluation of immunological response following a revaccination with a non-conjugated pneumococcal vaccine boosted or not by a conjugated pneumococcal vaccine in splenectomised patients (SPLENEVAC-2)Asplenic patients at risk for invasive pneumococcal diseasesMedDRA version: 20.0Level: PTClassification code 10041642Term: SplenectomySystem Organ Class: 10042613 - Surgical and medical proceduresEUCTR2018-003068-29-FRASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)56