Radiofrequency Probe for Management of Unresectable Bile Duct and Pancreatic Cancer (EndoHPB)
Primary Purpose
Pancreatic Cancer
Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Endoscopic Bipolar RadioFrequency Probe used to remove tumors in bile duct to manage Pancreatic Cancer
Sponsored by
About this trial
This is an interventional treatment trial for Pancreatic Cancer focused on measuring EndoHPB
Eligibility Criteria
Inclusion Criteria:
- Either gender greater than or equal to 18 years of age.
- Pancreatic Cancer or Cholangiocarcinoma unsuitable for surgical resection. Criteria of unresectability being based on 1) metastatic disease or 2) locally advanced disease.
- Biliary Obstruction
- Subjects capable of giving informed consent
- Life expectancy of at least 3 months
Exclusion Criteria:
- Cardiac Pacemaker
- Patient unstable for endoscopy
- Inability to give informed consent
- Uncorrected coagulopathy
- Pregnancy
- Karnofsky score less than 40%
Sites / Locations
Outcomes
Primary Outcome Measures
Improvement in size(patency of bile duct) measured by cholangiography or cholangioscopy, immediately post ablation
Secondary Outcome Measures
Full Information
NCT ID
NCT02042859
First Posted
January 15, 2014
Last Updated
January 20, 2014
Sponsor
Ochsner Health System
1. Study Identification
Unique Protocol Identification Number
NCT02042859
Brief Title
Radiofrequency Probe for Management of Unresectable Bile Duct and Pancreatic Cancer
Acronym
EndoHPB
Official Title
Pilot Study to Assess Safety and Efficacy Of An Endoscopic Bipolar Radiofrequency Probe (EndoHPB) In the Management of Unresectable Bile Duct and Pancreatic Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2014
Overall Recruitment Status
Unknown status
Study Start Date
February 2013 (undefined)
Primary Completion Date
February 2015 (Anticipated)
Study Completion Date
February 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ochsner Health System
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine whether the use of an FDA approved endoscopic bipolar catheter (EndoHPB) will ablate tissue in malignant tumors within the pancreatic ducts.
Detailed Description
Only a small proportion of patients with biliary obstruction caused by cholangiocarcinoma or pancreatic cancer are suitable for surgical resection. Therefore most patients with malignant biliary obstruction will need palliation of their jaundice to relieve the symptoms of pruritus, malabsorption, sepsis and to minimize potential hepatorenal complications. Restoring biliary flow with relief of jaundice is the primary goal in the palliation of obstructive biliary malignancy. Drainage at endoscopic retrograde cholangiopancreatography (ECRP) is established as a safer approach than at percutaneous transhepatic cholangiography (PTC) because it has a lower risk of bile leak, infection and hemorrhage. ECRP is the first approach to relieve malignant biliary obstruction but sometimes it is not technically possible to stent the patient by this approach, then a PTC needs to be undertaken. Self expanding mesh metal stents (SEMS) were introduced back in the 1990s. Problems can still arise with the use of covered stents such as cholecystitis, pancreatitis or tumor overgrowth at the end of the stent, and not all studies have shown that covered stents actually reduce the problems of tumor ingrowth and consequent stent occlusion. EndoHPB can be deployed via an ERCP or PTC route. By using radiofrequency (RF) energy to heat the tissue in the duct prior to insertion of the stent, the surrounding tissue becomes coagulated and this may may delay tumor growth and the time before the stent lumen becomes blocked. Thereby this allows increased periods between the need for intervention and further stent deployment. If EndoHPB use of luminal RF is demonstrated to be effective in luminal tumor ablation, it may have an additional role as a form of neoadjuvant therapy in cholangiocarcinoma and pancreatic cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
EndoHPB
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Endoscopic Bipolar RadioFrequency Probe used to remove tumors in bile duct to manage Pancreatic Cancer
Primary Outcome Measure Information:
Title
Improvement in size(patency of bile duct) measured by cholangiography or cholangioscopy, immediately post ablation
Time Frame
Baseline through visit 7
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Either gender greater than or equal to 18 years of age.
Pancreatic Cancer or Cholangiocarcinoma unsuitable for surgical resection. Criteria of unresectability being based on 1) metastatic disease or 2) locally advanced disease.
Biliary Obstruction
Subjects capable of giving informed consent
Life expectancy of at least 3 months
Exclusion Criteria:
Cardiac Pacemaker
Patient unstable for endoscopy
Inability to give informed consent
Uncorrected coagulopathy
Pregnancy
Karnofsky score less than 40%
12. IPD Sharing Statement
Learn more about this trial
Radiofrequency Probe for Management of Unresectable Bile Duct and Pancreatic Cancer
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