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NCT Number: NCT03000855

EUS - Guided Choledocho-duodenostomy Versus ERCP With Covered Metallic Stents in Patients With Unresectable Malignant Distal Common Bile Duct Strictures

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Royal Prince Alfred Hospital, Sydney, Australia

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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
  • Life expectancy < 3months

Treatment and study plan

EUS-guided choledocho-duodenostomy

Procedure

The CBD would be identified by a linear echoendoscope and a suitable puncture site in the bulb of the duodenum would be located. The common bile duct would be punctured with a 19-gauge needle and the position would be confirmed by aspiration of bile and contrast injection. A 0.025" or 0.035" guide wire would be passed through the needle in to the CBD. A fully covered metal stent would then be inserted after track dilation.

Endoscopic retrograde cholangiopancreatography with covered metallic stent

Procedure

After cannulation of the CBD, a cholangiography would be performed to assess the diameter of the CBD, the length and position of the biliary stricture. The endoscopist would decide on the appropriate size of SEMS to be placed. The stents should be visible from the duodenal lumen after deployment.

Primary outcomes

  1. stent patency rate

    Time frame: 1-year

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

Secondary outcomes

  1. Technical success

    Time frame: 1year

    Technical success is defined as the ability to access and drain the CBD by placement of a stent.

  2. Clinical success

    Time frame: 1 year

    Clinical success is defined as >30% drop in bilirubin levels

  3. Adverse events

    Time frame: 30 days

    Adverse events related to the endoscopic procedures would be graded according to the lexicon of endoscopic adverse events

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Collaborators

  • Kinki University
  • Tokyo Medical University

Registry information

Official study title

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

Acronym: DRAMBO

Important dates

Study start
2016
Primary completion
2021
Study completion
2022
First posted
Dec 22, 2016
Registry last updated
Aug 31, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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