IRCT2017032633143N1招募中2 期
Evalute and compare the effectiveness of oral thalidomide + Bortezomib (subcutaneous) + Dexamethasone(IV) regimen with Bortezomib (subcutaneous) + oral prednisolone + oral thalidomide regimen in patients with newly diagnosed multiple myeloma
Personal0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 30
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 70 years（—）
- 性别
- All
入选标准
- •Newly diagnosed patients with multiple myeloma who have over 18 years of age and are willing to participate in this study.
- •Exclusion criteria: HIV-positive patients, patients with a history of malignant, uncontrolled diabetes, neuropathy grade 2 diabetes, significant liver and kidney and heart failure are excluded.
排除标准
- 未提供
研究者
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