Cholangioscopic Assessment of Occluded Biliary Stent and Role of Biliary Radiofrequency Ablation
Primary Purpose
Obstructive Jaundice, Cholangitis
Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Single operator cholangioscopy, Endoscopic biliary RFA
Sponsored by
About this trial
This is an interventional diagnostic trial for Obstructive Jaundice focused on measuring obstructive Jaundice, Self Expandable Metal Stents (SEMS), Cholangitis
Eligibility Criteria
Inclusion Criteria:
- 1. Age 18 or older 2. Willing and able to comply with the study procedures and provide written informed consent to participate in the study 3. Recurrent biliary obstructive symptoms after biliary SEMS placement 4. Biliary SEMS occlusion.
Exclusion Criteria:
- 1. Contraindications for endoscopic techniques 2. Ongoing cholangitis. NOTE: In case a patient presents who meets the inclusion and exclusion criteria, but has cholangitis, then a naso-biliary drain (NBD) will be placed before the ERCP until the cholangitis resolves.
Sites / Locations
- Asian Institute of GastroenterologyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Sludge group
Ingrowth / Overgrowth
Arm Description
If Single operator cholangioscopy reveals only sludge then sludge will be cleared using conventional technique during ERCP.
If Single operator cholangioscopy reveals tumour ingrowth or overgrowth then to evaluate the role of biliary RFA for occluded stent due to tumour ingrowth or overgrowth
Outcomes
Primary Outcome Measures
Successful restoration of bile duct drainage
Successful restoration of bile duct drainage with biliary obstructive symptom and cholangitis relief as applicable, without procedure related SAE'S, from procedure through 30 days followup.
Secondary Outcome Measures
Resolution of cholangitis
1. Occurrence and severity of procedure related serious adverse events from procedure through 30 days after procedure 2. Resolution of cholangitis where applicable 4. Improvement of biliary obstructive symptoms at 1 week and 1 month post procedure compared to Baseline 5. Improvement of Laboratory Liver Function Tests (LFTs) at 1 week and 1 month post procedure compared to Baseline
Full Information
NCT ID
NCT03133026
First Posted
April 25, 2017
Last Updated
April 25, 2017
Sponsor
Asian Institute of Gastroenterology, India
1. Study Identification
Unique Protocol Identification Number
NCT03133026
Brief Title
Cholangioscopic Assessment of Occluded Biliary Stent and Role of Biliary Radiofrequency Ablation
Official Title
The Role of Cholangioscopy and Biliary Radio Frequency Ablation in the Management of Occluded Biliary Self-expanding Metal Stent.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Unknown status
Study Start Date
June 2016 (undefined)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
July 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Asian Institute of Gastroenterology, India
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Primary Objective: To document state-of- the-art multi-modality management of occluded biliary SEMS aiming to minimize number of reinterventions while providing symptom relief without procedure-related serious adverse events.
NOTE: This study will be hypothesis-generating for an anticipated randomized controlled study (RCT) to compare outcomes of placement of a plastic stent inside the occluded SEMS to outcomes of the proposed multi-modality approach.
Detailed Description
Study Design:
Prospective, multi-center, single arm, post market, observational study
Two groups:
Sludge group: SEMS occluded due to sludge/stones in SEMS
Ingrowth/overgrowth group: SEMS occluded due to malignant tumor ingrowth or benign hyperplastic tissue overgrowth
Primary Endpoint:
Successful restoration of bile duct drainage with biliary obstructive symptom and cholangitis relief as applicable, without procedure related SAE'S, from procedure through 30 days of follow-up.
Secondary Endpoints:
Occurrence and severity of procedure related serious adverse events from procedure through 30 days after procedure
Resolution of cholangitis where applicable
Technical success of procedure performed for restoration of bile duct drainage, overall and stratified by treatment group Sludge group: Ability to restore stent patency by cleaning the stent content followed by cholangiographically or cholangioscopically confirmed restored stent patency Ingrowth / overgrowth group: Ability to perform biliary radio frequency ablation (RFA) followed by cholangiographically or cholangioscopically confirmed restored stent patency
Improvement of biliary obstructive symptoms at 1 week and 1 month post procedure compared to Baseline
Improvement of Laboratory Liver Function Tests (LFT) at 1 week and 1 month post procedure compared to Baseline
Biliary Reintervention rate from procedure through 30 days after procedure, including reinterventions caused by plastic stent occlusion
Impact of cholangioscopy on current standard of care, which is to place a stent inside the occluded SEMS by
Avoiding placement of a second stent (plastic or metal)
Avoiding a repeat ERCP
Reducing associated cost
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Jaundice, Cholangitis
Keywords
obstructive Jaundice, Self Expandable Metal Stents (SEMS), Cholangitis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
4 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Sludge group
Arm Type
Active Comparator
Arm Description
If Single operator cholangioscopy reveals only sludge then sludge will be cleared using conventional technique during ERCP.
Arm Title
Ingrowth / Overgrowth
Arm Type
Active Comparator
Arm Description
If Single operator cholangioscopy reveals tumour ingrowth or overgrowth then to evaluate the role of biliary RFA for occluded stent due to tumour ingrowth or overgrowth
Intervention Type
Device
Intervention Name(s)
Single operator cholangioscopy, Endoscopic biliary RFA
Other Intervention Name(s)
SpyGlass cholangioscopy
Intervention Description
Single operator cholangioscopy will be done to acess the cause of occluded SEMS, if tumour ingrowth or overgrowth seen then endoscopic biliary RFA will be done
Primary Outcome Measure Information:
Title
Successful restoration of bile duct drainage
Description
Successful restoration of bile duct drainage with biliary obstructive symptom and cholangitis relief as applicable, without procedure related SAE'S, from procedure through 30 days followup.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Resolution of cholangitis
Description
1. Occurrence and severity of procedure related serious adverse events from procedure through 30 days after procedure 2. Resolution of cholangitis where applicable 4. Improvement of biliary obstructive symptoms at 1 week and 1 month post procedure compared to Baseline 5. Improvement of Laboratory Liver Function Tests (LFTs) at 1 week and 1 month post procedure compared to Baseline
Time Frame
1 week and 1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1. Age 18 or older 2. Willing and able to comply with the study procedures and provide written informed consent to participate in the study 3. Recurrent biliary obstructive symptoms after biliary SEMS placement 4. Biliary SEMS occlusion.
Exclusion Criteria:
1. Contraindications for endoscopic techniques 2. Ongoing cholangitis. NOTE: In case a patient presents who meets the inclusion and exclusion criteria, but has cholangitis, then a naso-biliary drain (NBD) will be placed before the ERCP until the cholangitis resolves.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohan Ramchandani, MD DM
Phone
9701335444
Email
ramchandanimohan@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohan Ramchandani, MD DM
Organizational Affiliation
Asian Institute of Gastroenterology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asian Institute of Gastroenterology
City
Hyderabad
State/Province
Telangana
ZIP/Postal Code
500082
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohan Ramchandani, MD DM
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Cholangioscopic Assessment of Occluded Biliary Stent and Role of Biliary Radiofrequency Ablation
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