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


N/A
18 Years
N/A
Open (Enrolling)
Both
Colorectal Cancer

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Trial Information

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


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.


Inclusion Criteria:



- Age 18 or above

- Diagnosed with CRC and prescribed with either XELOX for FOLFOX4 chemotherapy
treatment

Exclusion Criteria:

- 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

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Composite preparation, dispensing and administration time

Outcome Description:

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.

Outcome Time Frame:

Up to 6 months after the initiation of chemotherapy

Safety Issue:

No

Principal Investigator

Vivian WY Lee, PharmD

Investigator Role:

Principal Investigator

Investigator Affiliation:

CUHK

Authority:

Hong Kong: Ethics Committee

Study ID:

Roche-TR116581

NCT ID:

NCT01801085

Start Date:

October 2011

Completion Date:

August 2013

Related Keywords:

  • Colorectal Cancer
  • Time-and-Motion
  • Neoplasm
  • Colorectal Cancer
  • Colorectal Neoplasms

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