Case Series Study of Biliary Tract Cancer Patients in Japan

NCT ID: NCT01294085

Last Updated: 2011-11-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-11-30

Study Completion Date

2011-08-31

Brief Summary

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To assess the difference of prognosis between unresectable and recurrent biliary tract cancer and evaluate prognostic factors.

Detailed Description

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Most patients of biliary tract cancer have advanced disease at diagnosis and often relapse despite surgery. Combination therapy of gemcitabine and cisplatin could be a standard therapy for this kind of cancer with the evidence of phase III study compared with gemcitabine alone. However the prognosis and the tolerability of chemotherapy in the patients with recurrent biliary tract cancer after radical resection might differ from those of unresectable biliary tract cancer, because the dose intensity of chemotherapy can be influenced by adjuvant chemotherapy and/or hepatic resection.

Conditions

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Biliary Tract Cancer

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Unresectable or recurrent biliary tract cancer

Exclusion Criteria

* None
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kansai Hepatobiliary Oncology Group

NETWORK

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tatsuya Ioka, MD

Role: STUDY_DIRECTOR

Osaka Medical Center for Cancer and CVD

Locations

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Osaka Medical Center for Cancer and Cardiovascular Diseases

Osaka, , Japan

Site Status

Countries

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Japan

Other Identifiers

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UMIN000004530

Identifier Type: REGISTRY

Identifier Source: secondary_id

KHBO1001

Identifier Type: -

Identifier Source: org_study_id