Intensive Dose Tinzaparin in Hospitalized COVID-19 Patients (INTERACT)
Intensive Dose Tinzaparin in Hospitalized COVID19 Patients
調査の概要
詳細な説明
A prothrombotic state, attributable to a cytokine storm induced by severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) and leading to activation of the coagulation cascade, is a recognized feature of Coronavirus disease 2019 (COVID-19) infection. This can manifest in venous thromboembolism (VTE), arterial thrombosis events (ATE), and disseminated intravenous coagulation (DIC) and coagulopathy are reflective of more severe disease and adverse prognosis. A significant number of patients with COVID-19 require single or multiple organ support on the Intensive Care Unit (ICU), estimated to be between 12 and 17% of patients. with the reported mortality in these cohorts between 25 and 40%.
International guidelines recommend that hospitalized patients with COVID-19 should receive pharmacological prophylaxis against VTE, in the absence of contraindications. With respect to how VTE prophylaxis is achieved, Low Molecular Weight Heparins (LMWH), in addition to their well-known anticoagulant properties, appear to have additional antiviral and anti-inflammatory effects that may be potentially beneficial in hospitalized COVID-19 patients.
Though international and national guidelines state that all hospitalized patients with COVID-19 should receive pharmacologic thromboprophylaxis, the rising incidence of thrombotic complications in COVID-19 patients has led a lot of hospitals to adopt the strategy of increasing the dose of anticoagulation for prophylaxis to 'intermediate' or "therapeutic" doses using a risk-adapted strategy with increased doses administration based on factors associated with increased risk; clinicians weigh the benefits and risks of therapeutic anticoagulation in terms of thrombosis and major bleeding risk for individual patients.
Additionally, LMWHs have different physicochemical characteristics as a result of the diverse methods of their manufacturing. The variations in molecular composition and pharmacological properties of LMWHs are reflected in differences in their clinical efficacy and safety. Each LMWH should, therefore, be considered as a unique substance. Tinzaparin is the only LMWH known that is prepared by enzymatic hydrolysis with heparinase. Due to its preparation method, tinzaparin has distinct properties than other LMWHs including and not limited to: higher Anti-IIa activity and Anti-Xa/Anti-IIa activity ratio, the higher release of Tissue Factor Pathway Inhibitor (TFPI), less dependence from renal function for its clearance, and more complete neutralization from its antidote, if needed. Due to the key role of increased Thrombin generation (IIa) and Tissue factor (TF) pathway activation in COVID-19-associated thrombosis , special properties of tinzaparin in Anti-IIa activity and TFPI production and release from endothelial cells, as well as significant effects of TFPI in various vascular, inflammatory, cardiovascular, hematological and oncological disorders, tinzaparin could have an expanded role beyond its well-known anticoagulant function.
The purpose of this study is to evaluate the overall clinical effectiveness and safety of 'intermediate' or "therapeutic" doses of anticoagulation with tinzaparin administered for thromboprophylaxis in COVID-19 patients with moderate disease severity during hospitalization in Greek hospitals.
研究の種類
入学 (予想される)
連絡先と場所
研究連絡先
- 名前:Karolina Akinosoglou, MD,PhD
- 電話番号:+306977762897
- メール:akin@upatras.gr
研究場所
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Achaia
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Patras、Achaia、ギリシャ、26504
- 募集
- University Hospital of Patras
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コンタクト:
- Karolina Akinosoglou, Ass. Prof.
- 電話番号:+30 2610997254
- メール:akin@upatras.gr
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Attica
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Athens、Attica、ギリシャ、10676
- 募集
- Evangelismos General Hospital
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コンタクト:
- George Marakomichelakis, M.D. Ph.D.
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副調査官:
- Christine Vadala, M.D. Ph.D.
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Athens、Attica、ギリシャ、11522
- 募集
- General Hopital Elpis
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コンタクト:
- Spyridon Savvanis, M.D. Ph.D
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Epirus
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Ioannina、Epirus、ギリシャ、45500
- 募集
- University General Hospital Of Ioannina
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コンタクト:
- Haralampos ] Milionis, Ass. Prof.
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Ionian Islands
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Korfu、Ionian Islands、ギリシャ、49100
- 募集
- General Hospital of Kerkira "Ag. Irini"
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コンタクト:
- Ilias Papanicolaou, M.D. Ph.D.
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Macedonia
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Kozáni、Macedonia、ギリシャ、50100
- 募集
- General Hospital of Kozani "Mamatsio"
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コンタクト:
- Efthalia Randou, M.D. Ph.D.
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Peloponnese
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Patras、Peloponnese、ギリシャ、26335
- 募集
- Genereal Hospital of Patras "Ag. Andreas"
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コンタクト:
- George Efremidis, M.D. Ph.D.
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参加基準
適格基準
就学可能な年齢
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
- Patients admitted to hospital with COVID-19, PCR+ SARS-CoV-2 infection (from any specimen) administered thromboprophylaxis with tinzaparin in intermediate or therapeutic dose
- Age ≥ 18 years
- Signed informed consent
Exclusion Criteria
- Patients admitted to ICU with COVID-19, PCR+ SARS-CoV-2 infection (from any specimen)
- Age < 18 years
- Pregnancy
- Current diagnosis or suspicion of pulmonary thromboembolism or deep vein thrombosis
- Progression to death was imminent and inevitable within 24 hours from the admission, irrespective of the provision of treatments
- Not signed informed consent
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 |
介入・治療 |
|---|---|
|
COVID-19 patients
Patients admitted to hospital with COVID-19, PCR+ SARS-CoV-2 infection administered thromboprophylaxis with tinzaparin. Dosage: intermediate or therapeutic dose Frequency of tinzaparin administration: once daily Duration: Unknown |
Daily tinzaparin administration: 8000 - 14000 Anti-Xa IU
他の名前:
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Incidence of thrombotic events
時間枠:through study completion, an average of 6 months
|
Evaluate the incidence of thrombotic events: total & per type e.g.
PE, DVT, symptomatic, incidental, proximal, distant etc. (Measured as percentage of events in relation to the study population)
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through study completion, an average of 6 months
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Incidence of bleeding events
時間枠:through study completion, an average of 6 months
|
Evaluate τηε ιncidence of bleeding events (total & per type e.g.
Major, CRNMB and minor) (Measured as percentage of events in relation to the study population)
|
through study completion, an average of 6 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
WHO progression scale
時間枠:through study completion, an average of 6 months
|
Evaluate the patients in relation to World Health Organization (WHO) progression scale (range from 0 (healthy) to 10 (death); values below or equal to 5 correspond to the absence of any oxygen supply beside nasal or facial mask).
|
through study completion, an average of 6 months
|
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Length of hospital stay
時間枠:through study completion, an average of 6 months
|
Evaluate the length of hospital stay (in days)
|
through study completion, an average of 6 months
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協力者と研究者
捜査官
- 主任研究者:Karolina Akinosoglou, MD,PhD、University Hospital of Patras
出版物と役立つリンク
一般刊行物
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- Docherty AB, Harrison EM, Green CA, Hardwick HE, Pius R, Norman L, Holden KA, Read JM, Dondelinger F, Carson G, Merson L, Lee J, Plotkin D, Sigfrid L, Halpin S, Jackson C, Gamble C, Horby PW, Nguyen-Van-Tam JS, Ho A, Russell CD, Dunning J, Openshaw PJ, Baillie JK, Semple MG; ISARIC4C investigators. Features of 20 133 UK patients in hospital with covid-19 using the ISARIC WHO Clinical Characterisation Protocol: prospective observational cohort study. BMJ. 2020 May 22;369:m1985. doi: 10.1136/bmj.m1985.
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- Spyropoulos AC, Levy JH, Ageno W, Connors JM, Hunt BJ, Iba T, Levi M, Samama CM, Thachil J, Giannis D, Douketis JD; Subcommittee on Perioperative, Critical Care Thrombosis, Haemostasis of the Scientific, Standardization Committee of the International Society on Thrombosis and Haemostasis. Scientific and Standardization Committee communication: Clinical guidance on the diagnosis, prevention, and treatment of venous thromboembolism in hospitalized patients with COVID-19. J Thromb Haemost. 2020 Aug;18(8):1859-1865. doi: 10.1111/jth.14929. No abstract available.
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研究記録日
主要日程の研究
研究開始 (予想される)
一次修了 (予想される)
研究の完了 (予想される)
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 (実際)
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
追加の関連 MeSH 用語
その他の研究ID番号
- 18634/23-7-2021 pend. aprooval
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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