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Clinical Trials/JPRN-UMIN000002685
JPRN-UMIN000002685Completed未知

Feasibility study of outpatient chemotherapy with S-1+CDDP in gastric cancer patients - Feasibility study of outpatient chemotherapy with S-1+CDDP in gastric cancer patients

ational Cancer Center Hospital0 sites35 target enrollmentStarted: October 29, 2009Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
35

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 75years-old (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1) History of hypersensitivity to S-1 or CDDP. 2) Receiving fluoropyrimidine preparation. 3) Receiving systemic steroid therapy. 4) Required to continue to take flucytosine, phenytoin, and warfarin. 5) Severe complications (ileus, bowel obstruction, interstitial lung disease, uncontrolled diabetes, severe arrhythmia, heart failure, renal failure, liver cirrhosis, active hepatitis, and so on). 6) Active ischemic heart disease. 7) Woman who are pregnant, lactating, or willing to get pregnant, or man who are willing to have unprotected intercourse. 8) Severe mental disorder. 9) Regarded as inadequate physical conditions by attending physician.

Investigators

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