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Endoscopic Biliary Radiofrequency Ablation of Malignant Distal Common Bile Duct Strictures


2012-11


2017-12


2017-12


42

Study Overview

Endoscopic Biliary Radiofrequency Ablation of Malignant Distal Common Bile Duct Strictures

Malignant bile duct 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. To relieve obstructive jaundice as a result of the obstruction, endoscopic stent placement is usually required. The use self-expandable metal stents (SEMSs) have been shown to result in a longer patency times as compared with plastic stents. However, despite improvements in materials and stent design, stent obstruction still occurs in 13% to 44% of the patients. Tumor in-growth is the most common mechanism of stent obstruction. Recently, the use of endoscopic biliary radiofrequency ablation (EBRFA) have been described in patients suffering from inoperable malignant distal common bile duct (CBD) obstruction. The procedure uses heat energy to cause local tumour tissue death, resulting in re-opening of the bile duct lumen. The procedure has the potential of reducing the rate of stent obstruction after SEMS and also prolonging survival. The safety profile appears to be comparable that of placement of SEMS alone without added complications (<10%). The aim of the current study is to compare the efficacy of EBRFA with the addition of SEMS to SEMS alone in a randomized controlled trial.We hypothesize that the application of EBRFA can reduce recurrent biliary obstruction after SEMS.

N/A

  • Pancreatic Cancer
  • Cholangiocarcinoma
  • PROCEDURE: SEMS only
  • PROCEDURE: EBRFA and SEMS
  • CRE 2012.153

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2012-10-31  

N/A  

2018-01-24  

2012-11-01  

N/A  

2018-01-26  

2012-11-04  

N/A  

2018-01  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Treatment


Allocation:
Randomized


Interventional Model:
Parallel


Masking:
None


Arms and Interventions

Participant Group/ArmIntervention/Treatment
ACTIVE_COMPARATOR: SEMS only

Endoscopic retrograde cholangiopancreatography (ERCP) would be performed under standard operating conditions to confirm the length of the biliary stricture, diameter, and position. An uncovered self expanding metallic stent (SEMS) would be inserted to byp

PROCEDURE: SEMS only

  • The SEMS (Niti-S biliary uncovered metallic stent; Taewoong Medical, Korea) would be placed.
ACTIVE_COMPARATOR: EBRFA and SEMS

Endoscopic retrograde cholangiopancreatography (ERCP) would be performed under standard operating conditions to confirm the length of the biliary stricture, diameter, and position. The radiofrequency ablation (EBRFA) catheter would be placed under fluoros

PROCEDURE: EBRFA and SEMS

  • The radiofrequency ablation (RFA) catheter would be placed under fluoroscopic guidance across the biliary stricture. The Habib EndoHPB (EMcision UK, London, United Kingdom) radiofrequency ablation catheter is a bipolar RFA probe that is 8F (2.6 mm), 1.8 m
Primary Outcome MeasuresMeasure DescriptionTime Frame
Stent patency rate6 months
Secondary Outcome MeasuresMeasure DescriptionTime Frame
Overall survival3 years
Serious adverse events30 day
Unscheduled readmission rates1 year

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion Criteria:
    1. Age ≥ 18 years old with informed consent 2. Histologically (preferred) or radiologically confirmed distal malignant bile duct tumors 3. Inoperability by staging, comorbidities or patient wishes 4. Distal tumors 2cm away from the portal hilum 5. Bilirubin > 50umol/L at diagnosis
    Exclusion Criteria:
    1. Periampullary tumours 2. Multiple hepatic metastases with significant blockage of one or more liver segments (if no segment blockage, metastasis is not an exclusion criteria) 3. Presence of main portal vein thrombosis 4. Prior SEMS placement 5. Prior Billroth II or roux-en Y reconstruction 6. History of bleeding disorder or use of anticoagulation 7. Child's B/C cirrhosis 8. Pregnancy 9. Performance status ECOG ≥3 (confined to bed / chair > 50% waking hours) 10. Presence of other malignancy 11. Presence of gastric outlet obstruction 12. Life expectancy < 3months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Steel AW, Postgate AJ, Khorsandi S, Nicholls J, Jiao L, Vlavianos P, Habib N, Westaby D. Endoscopically applied radiofrequency ablation appears to be safe in the treatment of malignant biliary obstruction. Gastrointest Endosc. 2011 Jan;73(1):149-53. doi: 10.1016/j.gie.2010.09.031.