TCTR20230713001已完成3 期
Efficacy of Lower Dose of Dexamethasone Premedication in Patient Receiving Docetaxel-Based Chemotherapy in Preventing Hypersensitivity Reaction: A Randomized Controlled Trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 46
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •Patient receiving single agent Docetaxel tri-weekly regimen.
- •Patient has never received Docetaxel.
- •Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2.
- •Age 18 or older.
排除标准
- •Prostate cancer patient receiving Docetaxel with prednisolone for treatment.
- •Patient on steroid within 14 days prior to randomization.
- •Patient on immunosuppressive drug within 30 days prior to randomization.
- •Patient with severe allergic reaction such as, anaphylaxis, severe cutaneous adverse drug reaction (Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis (AGEP)).
- •Patient with history of hypersensitivity reaction grade 3 or higher to taxane based chemotherapy.
- •Patient with underlying disease diabetes mellitus.
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