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Clinical Trials/NCT02649712
NCT02649712
Completed
Not Applicable

Unilateral Stenting Versus Bilateral Stenting for Malignant Hilar Biliary Obstruction

Xuzhou Central Hospital1 site in 1 country72 target enrollmentJanuary 20, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cholangiocarcinoma
Sponsor
Xuzhou Central Hospital
Enrollment
72
Locations
1
Primary Endpoint
Stent patency (Stent dysfunction is suspected when the patient experiences recurrence of jaundice)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to compare the clinical effectiveness and long-term outcomes between patients with malignant hilar biliary obstruction who are treated by unilateral or bilateral stenting.

Detailed Description

Malignant hilar biliary obstruction is a common clinical manifestation and it can be caused by cholangiocarcinoma, gallbladder carcinoma, liver cancer, or other metastatic carcinoma. Most patients with malignant hilar biliary obstruction are unresectable at diagnosis. Biliary stenting has been widely used in palliative treatment of malignant hilar biliary obstruction. Hilar biliary obstruction usually involves the bifurcation of the biliary tract. Some researchers recommended unilateral stenting for malignant hilar biliary obstruction because drainage of 25% of entire liver can achieve the clinical success of biliary drainage. However, some researchers recommended bilateral stenting for malignant hilar biliary obstruction because some researches demonstrated that bilateral stenting can achieve a longer stent patency.In addition, there was no significant difference in post stenting survival between patients who were treated by unilateral or bilateral stenting. Therefore, it remains under debate whether unilateral or bilateral stenting is better in the treatment of malignant hilar biliary obstruction. The purpose of this study is to compare the clinical effectiveness and long-term outcomes between patients with malignant hilar biliary obstruction who are treated by unilateral or bilateral stenting.

Registry
clinicaltrials.gov
Start Date
January 20, 2016
End Date
October 31, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Xuzhou Central Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Malignant hilar biliary obstruction;
  • Unresectable cases

Exclusion Criteria

  • Bismuth I patients;
  • inability to obtain informed consent;
  • Eastern Cooperative Oncology Group performance status of 4;
  • severe dysfunction in other organs.

Outcomes

Primary Outcomes

Stent patency (Stent dysfunction is suspected when the patient experiences recurrence of jaundice)

Time Frame: From the date of randomization until the date of first documented stent dysfunction, assessed up to 10 months

Stent dysfunction is suspected when the patient experiences recurrence of jaundice.

Secondary Outcomes

  • Overall survival(From the date of randomization until the date of first documented death from any cause, assessed up to 12 months)
  • Stent dysfunction free-patient survival(From the date of randomization until the date of first documented stent dysfunction or the date of death from any cause, whichever came first, assessed up to 10 months.)

Study Sites (1)

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