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Phase 3
18 Years
70 Years
Open (Enrolling)
Both
Gastric Cancer

Thank you

Trial Information


Inclusion Criteria:



- informed consensus of patients

- be able to receive oral administration

- from 18 to 70 years old

- be proven to be primary adenocarcinoma of gastric cancer and pre-operative staging
cT4, any N,MO,

- without other chemotherapy and/or radiation against to the disease

- normal function of other organs including heart,liver ,kidney and so on

- Eastern Cooperative Oncology Group performance status:0~2

Exclusion Criteria:

- history of other malignancy

- allergic reaction to xeloda or oxaliplatin

- be enrolling in other clinical trials

- abnormal GI tract function

- dysfunction of other organs

- female in pregnancy or lactation,or refuse to receive Contraception measures during
chemotherapy

- other situation to be judged not adaptive to the study by investigators

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Total Survival

Outcome Time Frame:

5 years

Safety Issue:

No

Authority:

China:Clinical Trial Center

Study ID:

SYSUCCGPS2

NCT ID:

NCT01815853

Start Date:

July 2012

Completion Date:

Related Keywords:

  • Gastric Cancer
  • pre-operative,
  • chemoradiotherapy,
  • chemotherapy,
  • treatment
  • outcome
  • Stomach Neoplasms

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