Application of Medical Imaging Procedures in Surgery Implanting in Cancerology With the Aim to Reduce Invasive Acts (ATIM)
2011年6月21日 更新者：Centre Leon Berard
Aero digestive Cancer patients treated by external head and neck radiotherapy and/or by curie-therapy and/or mandible reconstruction by microanastomosed fibula flaps.
The purpose of the study is to Investigate the accuracy of implants insertion in the anteroposterior way, using radiosurgical guidance.
調査の概要
詳細な説明
- Investigate the accuracy of inserting implants in the vertical way and in angulation, on irradiated native mandible or on microanastomosed fibula flaps
- Investigate the accuracy of inserting implants in the anteroposterior way, in the vertical way and in angulation for all the involved patients (meaning on irradiated native mandible or on microanastomosed fibula flaps)
- Investigate the delay of mucous healing
- Estimate the prosthetic function
- Evaluate the osteonecrosis rate after radiation with traumatic etiology due to implantation
- Estimate the implant rate due to minimally invasive flaps
- Estimate the implant rate due to pure trans mucosa way
- Estimate the post surgical therapeutic success after 1 year
研究の種類
介入
入学 (予想される)
53
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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-
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Clermont-ferrand、フランス、63 000
- CHU Hôtel-Dieu Service d'Odontologie
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Lyon、フランス、69007
- Hospices Civils de Lyon Service de Consultations et Traitements Dentaires
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Pierre Benite、フランス、69495
- Centre Hospitalier Lyon Sud Service de Stomatologie et Chirurgie Maxillo-Faciale
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Cedex 08
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Lyon、Cedex 08、フランス、69373
- Centre Léon Bérard Service de Chirurgie-Stomatologie
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- age over 18
- Performance status over 70
- Histological evidence of upper digestive tract cancer
- History of cranial / facial radiotherapy or brachytherapy and/or microvascular fibula transfer.
- Bone volume sufficient to support an implant.
- Mandatory affiliation with a social security system
- Written, voluntary, informed consent
Exclusion Criteria:
- Patient with evolutive malignant disease
- Contraindication to general anesthesia
- Concurrent disease contra-indicating implant surgery (risk of infectious endocarditis, uncontrolled diabetes, HIV, evolutive neoplasia…)
- Patient enrolled in another clinical trial including chemotherapy
- Pregnant or lactating woman
- Anticipation of an impossible follow-up
- Patient deprived of freedom
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：支持療法
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
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 |
時間枠 |
|---|---|
|
Accuracy of implants insertion, radio-surgical guidance.
時間枠：8 months after inclusion
|
8 months after inclusion
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Accuracy of inserting implants
時間枠：16 months after inclusion
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16 months after inclusion
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Delay of mucous healing
時間枠：16 months after inclusion
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16 months after inclusion
|
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Estimation of the prosthetic function
時間枠：16 months after inclusion
|
16 months after inclusion
|
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Osteonecrosis rate after radiation with traumatic etiology due to implantation
時間枠：16 months after inclusion
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16 months after inclusion
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Implant rate
時間枠：16 months after inclusion
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16 months after inclusion
|
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Post surgical therapeutic success after 1 year
時間枠：after 1 year
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after 1 year
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者：Anne-Gaëlle BODARD, MD、Centre Léon Bérard
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
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研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始
2007年9月1日
一次修了 (予想される)
2011年12月1日
研究の完了 (予想される)
2011年12月1日
試験登録日
最初に提出
2009年6月2日
QC基準を満たした最初の提出物
2009年6月19日
最初の投稿 (見積もり)
2009年6月22日
学習記録の更新
投稿された最後の更新 (見積もり)
2011年6月22日
QC基準を満たした最後の更新が送信されました
2011年6月21日
最終確認日
2011年6月1日
詳しくは
本研究に関する用語
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