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临床试验/NCT01801085
NCT01801085终止不适用

The Impact of Nursing and Pharmacy Care Between Xeloda® and 5-Fluoruracil Regimens in the Management of Colorectal Cancer (CRC) in Hong Kong

Vivian Wing Yan Lee2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2011年10月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
21
试验地点
2
主要终点
Composite preparation, dispensing and administration time

研究概览

简要总结

This is a prospective time-and-motion study to document and compare the time used in preparation, dispensing and administration for capecitabine/oxaliplatin (XELOX) versus IV 5-FU/leucovorin/oxaliplatin (FOLFOX4) regimens in colorectal cancer (CRC) patients.

详细描述

Colorectal cancer (CRC) is the second most common cause of cancer-related death in Hong Kong. The traditional chemotherapy for CRC remains on intravenous (IV) fluorouracil (5-FU) based regimens with the response rates of 10-20% and a median survival of approximately one year. Recent years, oral chemotherapy has a more practical and economic advantages over IV regimen. It is understandable that patients prefer oral regimens as long as the clinical efficacy is maintained. Oral treatment strategy preserves quality of life for CRC patients. In a previous cost-minimization study conducted in Hong Kong, it was demonstrated that capecitabine was more cost-effective than 5-FU plus oxaliplatin assuming they had equal clinical efficacy. Not only is capecitabine more cost-effective, it may also have additional cost saving in the nursing and pharmacy time . It is because a significant amount of time can be saved in both nursing and pharmacy for the preparation and administration of IV chemotherapy. In the UK, it was demonstrated that capecitabine required less pharmacy and administration time per cycle than 5-FU based IV chemotherapy. However, there is a lack of local data to demonstrate the impact of pharmacy and nursing care utilizing capecitabine comparing to traditional IV chemotherapy in CRC patients of Hong Kong.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or above
  • Diagnosed with CRC and prescribed with either XELOX for FOLFOX4 chemotherapy treatment

排除标准

  • Patients less than 18 years of age
  • Persons related unequally to investigators
  • Patients who are mentally/cognitively disabled
  • Patients who refuse to give consent to participate

结局指标

主要结局

Composite preparation, dispensing and administration time

时间窗: Up to 6 months after the initiation of chemotherapy

Composite time is measured via real-time recording. Total length of the said time points are to be recorded using a stop-watch and the sum is tabulated in the end.

次要结局

  • Capital item utilization (hospital bed and infusion pump)(Up to 6 months after the initiation of chemotherapy)

研究者

发起方
Vivian Wing Yan Lee
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Vivian Wing Yan Lee

Associate Professor

Chinese University of Hong Kong

研究点 (2)

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