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Clinical Trials/NCT03000855
NCT03000855
Completed
Phase 2

EUS - Guided Choledocho-duodenostomy Versus ERCP With Covered Metallic Stents in Patients With Unresectable Malignant Distal Common Bile Duct Strictures. A Multi-centred Randomised Controlled Trial

Chinese University of Hong Kong6 sites in 5 countries77 target enrollmentDecember 2016

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Malignant Biliary Obstruction
Sponsor
Chinese University of Hong Kong
Enrollment
77
Locations
6
Primary Endpoint
stent patency rate
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

EUS - guided choledocho-duodenostomy (ECDS) is an established option for bile duct drainage in unresectable malignant distal CBD strictures when endoscopic retrograde cholangiopancreatography (ERCP) fails. However, how primary ECDS compares with ERCP with covered self-expanding metallic stents (CSEMS) in unresectable malignant distal CBD strictures is uncertain.

The aim of the current study is to compare primary ECDS versus ERCP with CSEMS in unresectable malignant distal CBD strictures. We hypothesis that ECDS is associated with a higher 1-year stent patency rate.

Detailed Description

Malignant biliary obstruction is a common sequela of pancreatic cancers or distal bile duct cancers, and its development can hinder the use of chemotherapy, decrease patient quality of life and decrease survival. Malignant biliary obstruction is traditionally palliated with ERCP with metallic stent insertion. However, these stents are prone to obstruction due to tumour ingrowth. In addition, ERCP may not always be possible due to tumour obstruction and percutaneous biliary drainage may be required. Recently, ECDS has been described as an alternative to percutaneous biliary drainage in patients with failed ERCP. The procedure is also associated with potential advantages as compared to conventional ERCP. In particular, the risk of tumour ingrowth into the stent placed after ECDS is low and stent patency rates may be better than ERCP. Thus, the aim of the current study is to compare primary ECDS versus ERCP with CSEMS in unresectable malignant distal CBD strictures.

Registry
clinicaltrials.gov
Start Date
December 2016
End Date
December 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Anthony Teoh

Honorary Associate Professor

Chinese University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years old with informed consent
  • Histologically (preferred) or radiologically confirmed distal malignant bile duct tumors
  • Inoperability by staging, comorbidities or patient wishes
  • Distal tumors 2cm away from the portal hilum
  • Bilirubin \> 50umol/L at diagnosis

Exclusion Criteria

  • Multiple hepatic metastases with significant blockage of one or more liver segments (if no segment blockage, metastasis is not an exclusion criteria)
  • Presence of main portal vein thrombosis
  • Prior SEMS placement
  • Intraductal papillary mucinous carcinomas
  • Prior Billroth II or roux-en Y reconstruction
  • History of bleeding disorder or use of anticoagulation
  • Child's B/C cirrhosis
  • Pregnancy
  • Performance status ECOG ≥3 (confined to bed / chair \> 50% waking hours)
  • Presence of other malignancy

Outcomes

Primary Outcomes

stent patency rate

Time Frame: 1-year

Stent dysfunction is defined as radiology or endoscopy confirmed stent obstruction.

Secondary Outcomes

  • Clinical success(1 year)
  • Technical success(1year)
  • Adverse events(30 days)

Study Sites (6)

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