抄録
Standard therapy for idiopathic thrombocytopenic purpura (ITP) has not been established. We are conducting a multicenter, prospective trial to determine the efficacy and safety of short-term, high-dose dexamethasone therapy in ITP patients aged 18-80 years with platelet counts of < 20, 000 /μL, or with < 50, 000/ μL and bleeding symptoms. The primary endpoints of this trial are the proportion of responses (complete plus partial response) on day 180 (day 46+180) after the completion of the 46-day high-dose dexamethasone therapy. The results of this investigation of the effectiveness and safety of this regimen will be essential for the establishment of standard therapy for ITP.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 197-201 |
| ページ数 | 5 |
| ジャーナル | Acta Medica Okayama |
| 巻 | 72 |
| 号 | 2 |
| 出版ステータス | 出版済み - 2018 |
| 外部発表 | はい |
All Science Journal Classification (ASJC) codes
- 生化学、遺伝学、分子生物学一般
フィンガープリント
「High-dose dexamethasone therapy as the initial treatment for idiopathic thrombocytopenic purpura: Protocol for a multicenter, open-label, single arm trial」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。引用スタイル
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