Vitamin E to Prevent Mucositis in Children With Cancer
Serial Controlled N-of-1 Trials of Topical Vitamin E as Prophylaxis for Chemotherapy-induced Oral Mucositis in Pediatric Patients
調査の概要
詳細な説明
Oral mucositis is a common consequence of chemotherapy and is an important sequela of cancer therapy because it is painful and affects quality of life, may lead to hospitalization for hydration or pain control, and provides a portal of entry for oral microflora. In addition, oral mucositis has become a major dose-limiting toxicity and consequently, may limit delivery of anti-cancer therapy.
Despite the frequency of mucositis, there are no feasible therapies proven to be successful in preventing mucositis in children. Vitamin E is a fat-soluble essential vitamin that may protect against doxorubicin-induced oral mucositis through its anti-oxidant properties.
In this study, we will examine the efficacy of topical vitamin E as prophylaxis against chemotherapy-induced mucositis with a novel methodology appropriate for the study of rare conditions, namely combining N-of-1 trials using Bayesian meta-analysis.
The primary outcome is an objective mucositis score measured on days 7, 10, 14 and 17. Secondary outcomes included daily pain and swallowing visual analogue scale scores, and World Health Organization mucositis scores collected on days 5 to 20.
Comparisons: Objective and subjective mucositis scores will be compared in cycles associated with topical vitamin E versus cycles associated with placebo administration. We will use repeated measures analysis within a Bayesian framework in order to conduct this comparison.
研究の種類
入学
段階
- フェーズ2
- フェーズ 3
連絡先と場所
研究場所
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Ontario
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Toronto、Ontario、カナダ、M5G 1X8
- The Hospital for Sick Children
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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
説明
Inclusion Criteria:
- diagnosis of cancer and treated at the Hospital for Sick Children, Toronto, Canada
- planned chemotherapy includes at least two identical courses of doxorubicin-containing chemotherapy in which the dose of doxorubicin was at least 60 mg/m2 per course
- at least 6 years of age and less than 18 years
- lives in the Greater Toronto area
Exclusion Criteria:
- allergy to vitamin E or placebo ingredients
- child is unable to comply with topical vitamin E application
- cild is receiving head or neck irradiation
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
- 主な目的:防止
- 割り当て:ランダム化
- 介入モデル:クロスオーバー割り当て
- マスキング:ダブル
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 |
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Objective mucositis score at 7, 10, 14, and 17 days post initiation of chemotherapy
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二次結果の測定
結果測定 |
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Pain visual analogue scale
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Difficulty swallowing visual analogue scale
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World Health Organization mucositis grade
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Analgesia use (topical, systemic non-narcotic or narcotic
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Receipt of intravenous fluid, and total parenteral nutrition.
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Chemotherapy decrements or delays due to mucositis
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協力者と研究者
捜査官
- 主任研究者:Brian M Feldman, MD, MSc、The Hospital for Sick Children
研究記録日
主要日程の研究
研究開始
研究の完了
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
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