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临床试验/TCTR20240319009
TCTR20240319009招募中2 期

Efficacy of High Dose Dexamethasone in Prevention of Hypersensitivity Reaction Induced by Oxaliplatin: A Randomized Double-Blind Controlled Trial

Sisaket Hospital0 个研究点目标入组 194 人开始时间: 2024年3月19日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
194

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

  • 1. Patients with cancer, aged at least 18 years, diagnosed with colorectal cancer who have received oxaliplatin
  • 2. In the case of metastatic disease, participants must not have received oxaliplatin before
  • 3. In the case of adjuvant oxaliplatin treatment, it must be stopped at least 6 months before entering the study
  • 4. ECOG performance status 0-2
  • 4. Life expectancymmore than 12 weeks
  • 5. Blood test results: ANC more than 1,000/mm3, platelet more than 75,000, Hb more than 8 g/dL, total bilirubin more than 2, Cr less than 1.5 times the upper normal limit
  • 6. Patients who have signed informed consent to participate in the research project

排除标准

  • 1. Patients with a history of severe allergic reactions to oxaliplatin or other platinum-containing compounds
  • 2. Patients with severe hypersensitivity to other drugs or excipients in the study drug
  • 3. Patients with uncontrolled underlying diseases
  • 4. Patients with multiple primary cancers in the past 5 years
  • 5. Patients with pleural effusion, pericardial effusion, or ascites that require drainage
  • 6. Patients with significant mental or psychological illness

研究者

发起方
Sisaket Hospital

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