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Clinical Trials/JPRN-UMIN000012293
JPRN-UMIN000012293
Completed
Phase 2

eoadjuvant radiation therapy concurrent with S-1 followed by systemic Gemcitabine therapy for Borderline resectable pancreatic cancer patients; A phase2 study - A phase2 study of neoadjuvant S1+RT followed by systemic Gem therapy for Borderline resectable pancreatic cancer patients

Hokkaido Pancreatic Cancer Study Group (HOPS)0 sites45 target enrollmentNovember 15, 2013

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Hokkaido Pancreatic Cancer Study Group (HOPS)
Enrollment
45
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 15, 2013
End Date
April 28, 2017
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Hokkaido Pancreatic Cancer Study Group (HOPS)

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) treatment history of a pancreatic cancer (chemotherapy, radiotherapy, surgical) 2\) treatment history of other malignant tumors (chemotherapy, radiotherapy) 3\) Patients who can' t receive neither iodic drug because of drug allergy 4\) Including in an exposure field is impossible with contrast enhanced CT 5\) Massive pleural or abdominal effusion 6\) Pleural membranes and peritoneum sowing are proved by cytological diagnosis 7\) Existence of tumor exposure with CT or Endoscope 8\) Hemorrhagic peptic ulcer 9\) Watery diarrhea 10\) Regular use of frucitocin, fenitoin or warfarin 11\) Lung fibrosis or intestinal pneumonia, and anamnesis or imaging findings 12\) Severe infection 13\) Serious complications (e.g. heart failure, hepatic failure, intestinal paralysis, intestinal obstruction) 14\) Uncontrolled diabetes 15\) Simultaneous or metachronous (within 3 years) double cancers 16\) Patients requiring systemic steroids medication 17\) Severe mental illness 18\) Severe drug hypersensitivity 19\) Males that are currently attempting to produce a pregnancy 20\) Pregnant females, possibly pregnant females, females wishing to become pregnant 21\) Patients seems inadequate for this study by investigators

Outcomes

Primary Outcomes

Not specified

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