跳至主要内容
临床试验/NCT01942200
NCT01942200已完成不适用

Open, Multicenter Observational Study of Oxaliplatin Utilized in Combination Therapy for Adjuvant Treatment of Colon Carcinoma of Stage III After Complete Removal of the Primary Tumor and for Treatment of Metastasizing Colorectal Carcinoma.

Onkovis GmbH1 个研究点 分布在 1 个国家目标入组 383 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Onkovis GmbH
入组人数
383
试验地点
1
主要终点
The Quantity of Oxaliplatin onkovis needed per treatment cycle

研究概览

简要总结

The main purpose of this observational study with Oxaliplatin onkovis is to determine the number of treatment cycles and the quantity of Oxaliplatin onkovis needed for this purpose under the special circumstances of ambulant chemotherapy.

Onkovis aims to contribute to an economical utilization of the chemotherapeutics. This includes provision of appropriate packaging sizes to decrease the excess quantity to be discarded, and thus also follows this objective.

Secondary objective is the assessment of the side effects of Oxaliplatin onkovis. To this end, data regarding co-medication and adverse events are also collected.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Indication for Oxaliplatin according to the Summary of Product Characteristics (SmPC) and treating physician

排除标准

  • According to the Oxaliplatin SmPC

结局指标

主要结局

The Quantity of Oxaliplatin onkovis needed per treatment cycle

时间窗: up to 24 weeks

Determine the quantity of Oxaliplatin onkovis needed per treatment cycle

次要结局

  • Adverse events during and after treatment(up to 24 weeks)

研究者

发起方
Onkovis GmbH
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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