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Clinical Trials/JPRN-UMIN000019611
JPRN-UMIN000019611
Completed
未知

Phase II trial of nab-paclitaxel and carboplatin with concurrent radiotherapy for patients with locally advanced non-small cell lung cancer - Phase II trial of nab-paclitaxel and carboplatin with concurrent radiotherapy for patients with locally advanced non-small cell lung cancer

Department of Radiation Oncology, Yamaguchi University Hospital0 sites37 target enrollmentNovember 2, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
non-small cell lung cancer
Sponsor
Department of Radiation Oncology, Yamaguchi University Hospital
Enrollment
37
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 2, 2015
End Date
April 26, 2017
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Department of Radiation Oncology, Yamaguchi University Hospital

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Patient with a history of allergy to taxane antineoplastic agents 2\. Patient with a history of allergy to carboplatin or other platinum\-based antineoplastic agents 3\. Patient with a history of allergy to albumin 4\. without the concent to the risk of infection caused by albumin preparation 5\. Patients with active infection 6\. Patients with serious complications (e.g. heart failure, severe pulmonary emphysema, renal disfunction, hepatic disfunction, poorly controlled diabetes or hypertension) 7\. Patient with severe bone marrow suppression 8\. Patient with active double cancer within 5years prior to the study 9\. Patients with pleural or pericardial effusion, or ascites. 10\. Patient with motor paralysis or neuropathy, except due to NSCLC 11\. Exhibiting significant interstitial pneumonitis, or pulmonary fibrosis in the chest radiograph 12\. Patient with collagen vascular diseases 13\. Female Patient in or having a chance or planning of pregnancy or breast feeding 14\. Male patient in planning to impregnate 15\. Inappropriate patients for this study judged by the attending physician

Outcomes

Primary Outcomes

Not specified

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