The Role of FDG-PET/CT Imaging in the Management of Patients With Thromboembolic Disorders (The PETVET Study) (PETVET)
The Role of FDG-PET/CT Imaging in the Management of Patients With Thromboembolic Disorders
調査の概要
状態
条件
詳細な説明
Acute DVT and PE are common and serious conditions. Highly effective treatment (most often anticoagulant agents) is available for acute VTE, but it is associated with potentially dangerous side effects. In addition, DVT and PE are just two manifestations of VTE, which can occur everywhere in the human organism. An underlying disease (i.e. cancer) is often a key factor in developing VTE.
Commonly used diagnostic imaging techniques in DVT and PE have a fair diagnostic accuracy, but do not address other important aspects of the disease. In contrast to this, FDG-PET/CT has the potential to contribute in VTE diagnosis by
- Differentiate between acute and chronic VTE
- Screening of the entire body for VTE (e.g. the pelvis where normal imaging techniques fail)
- Early diagnosis of underlying disease (e.g. cancer, with the possibility of early treatment)
This is a pilot study with the above mentioned objectives, and is part of a larger study addressing other aspects of FDG-PET/CT in VTE.
The investigators believe that their hypothesis that FDG-PET/CT imaging may introduce a new approach for detecting thrombi anywhere in the body, particularly in the venous system including the pelvis and the calves, will add a new dimension in treating patients with suspected PE. This technology will only detect acute thrombi and not chronic thrombi that no longer have activity, which will obviate unnecessary treatment in this population.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Odense、デンマーク、dk-5000
- Dept. of Acute Medicine, Odense University Hospital
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Odense、デンマーク、dk-5000
- Dept. of Nuclear Medicine, Odense University Hospital
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Odense、デンマーク、dk-5000
- Dept. of Respiratory Medicine, Odense University Hospital,
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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:
- Positive or negative diagnosis of VTE (DVT/PE)
- Age ≥ 50 years
- Informed consent obtained
- Symptoms < 1 week
Exclusion Criteria:
- Pregnant or lactating women
- Foreign language patients with a need for an interpreter
- Previous DVT or PE
- Known malignancy
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
- 観測モデル:ケースコントロール
- 時間の展望:見込みのある
コホートと介入
グループ/コホート |
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DVT confirmed
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DVT ruled out
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PE confirmed
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PE ruled out
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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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Proof-of-concept
時間枠:During diagnostic workup
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Simple assessment of scans - positive or negative in the relevant patient categories
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During diagnostic workup
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協力者と研究者
捜査官
- スタディチェア:Soeren Hess, MD、Odense University Hospital
- スタディチェア:Poul Henning Madsen, MD、Odense University Hospital
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 (見積もり)
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
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。