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临床试验/ACTRN12616001536459
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

发起方
MidCentral Regional Cancer Treatment Services

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