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Clinical Trials/JPRN-UMIN000016226
JPRN-UMIN000016226
Completed
未知

Prospective observational study on the efficacy and safety of EPA in advanced gastric cancer patients treated by S-1+CDDP as first line. - Prospective observational study on the efficacy and safety of EPA in advanced gastric cancer patients treated by S-1+CDDP as first line.

Kyushu medical center, medical oncology0 sites30 target enrollmentJanuary 15, 2015
Conditionsgastric cancer

Overview

Phase
未知
Intervention
Not specified
Conditions
gastric cancer
Sponsor
Kyushu medical center, medical oncology
Enrollment
30
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 15, 2015
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Kyushu medical center, medical oncology

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\)Patients with active bleeding or beedingtendency (2\)Patients who receive anticoagulant or antiplatelet drug (3\)Patients without prior therapy with drugs or supplements contained icosapentaenoic acid (4\)Patients with a history of allergy to icosapentaenoic acid (5\)Patients scheduled for surgery (6\)Patients scheduled for immune therapy (7\)Patients with serious complication (8\)Patients with immune\-mediated illness (9\)Patients with digestive symptom by ileus or gastrointestinal bleeding (10\)Patients with symptomatic brain metastases or carcinomatous meningitis (11\)Patients with massive pericardial effusion, pleural effusion or ascites \*except for patients if effusions and ascites did not accumulate for more than two weeks after dranage therapy \*include patients if pleurosclerosis was performed with anticancer drugs except OK\-432 (12\)Metachronous and synchronous double cancer (13\)Bood tests positive for HBs antigen (14\)Patients who receive continuous corticosteroid administration (15\)Patients who receive drugs interact with S\-1 or cisplatin (16\)Uncontrolled psychiatry disease (17\)Pregnant or lactating female and men who want to get partner pregnant (18\)Judged inappropriate by the investigators

Outcomes

Primary Outcomes

Not specified

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