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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01862276
Other study ID # KHBO1206
Secondary ID UMIN000010416
Status Completed
Phase N/A
First received May 14, 2013
Last updated June 29, 2014
Start date March 2013
Est. completion date March 2014

Study information

Verified date June 2014
Source Kansai Hepatobiliary Oncology Group
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Observational

Clinical Trial Summary

To investigate the prognosis due to presence or absence of bile duct resection in intrahepatic cholangiocarcinoma that require hepatic lobectomy.


Description:

The bile duct resection in hepatic lobectomy due to cholangiocarcinoma, mass forming type, is still controversial. We retrospectively evaluated the effect of bile duct resection in this surgery.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Cases of major hepatectomy due to intrahepatic cholangiocarcinoma

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Locations

Country Name City State
Japan Osaka University, Graduate School of Medicine Osaka

Sponsors (1)

Lead Sponsor Collaborator
Kansai Hepatobiliary Oncology Group

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary 3-year recurrence-free survival rate 11 years (2000-2010) No
Primary Ratio of local recurrence at the hepatico-duodenal ligament 11 years No
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