Influenza Virus - A Multicenter Registry
INFLUENZA VIRUS INFECTIONS IN TRANSPLANT RECIPIENTS: A MULTICENTER REGISTRY
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Alberta
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Edmonton、Alberta、カナダ
- University of Alberta Hospital
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Edmonton、Alberta、カナダ、T6G 2E1
- University of Alberta Hospital
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参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
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influenza infection
Patients with the diagnosis of influenza infection by standard laboratory technique
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協力者と研究者
スポンサー
捜査官
- 主任研究者:Deepali Kumar, MD、University of Alberta
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- UOA-FLU-2010-11
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。