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Clinical Trials/JPRN-UMIN000002937
JPRN-UMIN000002937
Completed
Phase 2

Phase II study of concurrent chemoradiotherapy with weekly cisplatin and paclitaxel chemotherapy for locally advanced cervical carcinoma (JACCRO GY-01) - Phase II study of concurrent chemoradiotherapy with weekly cisplatin and paclitaxel chemotherapy for locally advanced cervical carcinoma (JACCRO GY-01)

Japanese Cancer Clinical Research Organization(JACCRO)0 sites70 target enrollmentDecember 24, 2009

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
terine cervical carcinoma
Sponsor
Japanese Cancer Clinical Research Organization(JACCRO)
Enrollment
70
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 24, 2009
End Date
November 1, 2013
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Japanese Cancer Clinical Research Organization(JACCRO)

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Patient with stump cancer 2\) Patient who has an active infection. 3\) Patient who has a hydronephrosis. 4\) Patient who has myocardial infarction, unstable angina and uncontrolled irregular heartbeat within six months before registration. 5\) Patient who has a serious complication. 6\) Patient who has a radiotherapy history in the pelvic region. 7\) Patient who has an active double cancer. However, cancers in situ that are considered as recovered by local treatment or legions equivalent to intramucosal cancer are not included in the active double cancers. 8\) Patient who underwent exploratory laparotomy for cervical cancer. 9\) Patient who is complicated by mental disease or psychological symptom and considered difficult to participate in the test. 10\) Patient who is pregnant or of child\-bearing potential or breast\-feeding. 11\) Patient who is diagnosed as a pyometra and there is no improvement in pyometra and infection despite the implementation of appropriate measures. 12\) Other cases where doctors in attendance consider patients inappropriate.

Outcomes

Primary Outcomes

Not specified

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