Influenza Virus - A Multicenter Registry
INFLUENZA VIRUS INFECTIONS IN TRANSPLANT RECIPIENTS: A MULTICENTER REGISTRY
研究概览
详细说明
This study will be a prospective, multi-center study conducted at investigator sites who comprise the Influenza in Transplant collaborative study group. This includes over 30 centers from across North America and Europe. The co-ordinating center will be the University of Alberta. We will aim to enrol 300 patients in the registry over a 3 year period.
The following information will be gathered:
Clinical Information
- Baseline demographic information about the transplant (including immunosuppression, graft function)
- Comorbidities such as diabetes, obesity, chronic lung disease
- Symptoms of infection, radiologic features of infections
- Antiviral use
- History of vaccination
- Outcomes such as hospitalization, ICU admission, mechanical ventilation, death
- Long term outcomes: allograft function, chronic respiratory disease
- Laboratory parameters including lymphocyte count, immunoglobulin levels, renal function
- Adverse events - all serious adverse events occurring during the study (till day 180) will be reported. These include: a) hospitalization; b) congenital deformity; c) death; d) disability; and e) other adverse events the investigator considers serious. Pregnancy during the follow-up period will also be reported.
Virology
- Method of diagnosis (DFA, viral culture, PCR)
- Subtype of influenza virus (ie HxNx)
- Viral Shedding by serial NP swabs at day 0 (diagnosis), 3, 6, 11, 18, 28 (weekly thereafter if shedding persists)
- Quantitative PCR of NP swabs (centrally at University of Alberta)
- Antiviral resistance testing at first and last positive swabs
Immunology - Serum collection at disease onset and 4-6 weeks afterwards for
- Serology against circulating influenza viruses
- Production of HLA alloantibodies
Significance:
Despite the recognized importance of influenza in transplant patients, there is actually very limited prospective data. This registry will represent the largest prospective data collection on influenza in transplant patients and will provide invaluable data on the clinical presentations, antiviral efficacy and other parameters related to influenza.
研究类型
注册 (实际的)
联系人和位置
学习地点
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Alberta
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Edmonton、Alberta、加拿大
- University of Alberta Hospital
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Edmonton、Alberta、加拿大、T6G 2E1
- University of Alberta Hospital
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参与标准
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Solid organ transplant recipients on at least one immunosuppressive medication
- Hematopoietic stem cell transplant recipients - allogeneic or autologous
- Pediatric or Adult
- Diagnosis of influenza infection by standard laboratory technique
Exclusion Criteria:
not able to comply with the protocol
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
|---|
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influenza infection
Patients with the diagnosis of influenza infection by standard laboratory technique
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合作者和调查者
调查人员
- 首席研究员:Deepali Kumar, MD、University of Alberta
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.