ACTRN12616001536459招募中2 期
Oxaliplatin Dose Modification for Colorectal Cancer Triggered by Patient Reported Toxicity: Acceptability and Effect on Chronic Chemotherapy Induced Peripheral Neuropathy
MidCentral Regional Cancer Treatment Services0 个研究点目标入组 30 人开始时间: 2016年11月8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
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Prevention
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •1.Male or female patients with histologically proven colorectal adenocarcinoma
- •* Histological confirmation of metastatic disease or of the primary lesion where an alternative cause for metastatic disease is considered unlikely
- •2.Unresectable metastatic disease with radiological measurable disease according to RECIST v1.1 on computed tomography (CT)
- •3.Assessed as suitable for palliative XELOX chemotherapy
- •4.No contraindications to capecitabine or oxaliplatin chemotherapy
- •5.Able to complete questionnaires and comply with intervention, assessments and follow-up
- •6.Written, informed consent
排除标准
- •1.Age < 18 years
- •2.Patients with a pre-existing neurological condition including established diabetic peripheral neuropathy
- •3.Patients who have previously been treated with neurotoxic chemotherapy agents including platinums, taxanes and vinka-alkaloids
- •4.Patients with contra-indications to capecitabine or oxaliplatin
研究者
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