search
Back to results

Percutaneous Endoluminal Benign Biliary Laser (PEBBL)

Primary Purpose

Benign Biliary Strictures With Current or Prior Biliary Obstruction

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Percutaneous transhepatic cholangioscopic (PTCS) laser incision
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Biliary Strictures With Current or Prior Biliary Obstruction

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with a diagnosis of Benign Biliary Strictures (BBS)
  2. Clinical and/or laboratory evidence of biliary obstruction (current or prior)
  3. Age 18 years or older at the time of intervention

Exclusion Criteria:

  1. Patients with a diagnosis of malignant biliary stricture at the time of enrollment
  2. Patients who are subsequently diagnosed with malignant biliary stricture during the study period
  3. Liver transplantation within the last 90 days
  4. Active cholangitis or sepsis
  5. Emergent need for biliary decompression
  6. Patients with a diagnosis of primary sclerosing cholangitis with presence of 3 or more strictured segments
  7. Patients with a life-expectancy of less than 36 months

Sites / Locations

  • University of California Los AngelesRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patients with benign biliary strictures

Arm Description

Patients with benign biliary strictures with current or prior biliary obstruction, who would otherwise receive standard treatment with long-term biliary tube drainage.

Outcomes

Primary Outcome Measures

Incidence of Post Procedure Adverse Events
Safety evaluated by cumulative rates of post-interventional complications after PTCS-guided laser incision. Complications will be reported according to the Society of Interventional Radiology Adverse Event (AE) classification system. Safety will be reported as 30-day composite of all post-procedure AEs. Complications will be further qualified and quantified by AE severity category and individual AE types.
Feasibility of Procedure
Feasibility evaluated by technical success of PTCS-guided laser incision. a. Technical success defined as endoscopic and cholangiographic evidence of improved patency at the time of intervention.

Secondary Outcome Measures

Primary Bile Duct Patency
Primary bile duct patency evaluated as mean time to first stricture recurrence. Stricture recurrence will be defined as clinical and/or radiographic evidence of biliary occlusion requiring additional therapy. The date of PTCS or post-intervention biliary catheter removal will mark the time of initiation.
Tube-Free Survival
Tube-free survival evaluated as cumulative time survived without a biliary device during the study period. Duration of time that patients require a biliary catheter or stent during follow-up period will be subtracted from the 12-month total. If a device is subsequently removed, tube-free survival time will continue to be accrued up to 12 months post-treatment.
12-Month Cumulative Complications
12-month cumulative complications from laser treatment or recurrent biliary disease. a. Composite of all PTCS- and stricture-related AEs during the 12-month follow-up period.

Full Information

First Posted
September 30, 2022
Last Updated
October 7, 2022
Sponsor
University of California, Los Angeles
Collaborators
Boston Scientific Corporation
search

1. Study Identification

Unique Protocol Identification Number
NCT05567003
Brief Title
Percutaneous Endoluminal Benign Biliary Laser
Acronym
PEBBL
Official Title
Percutaneous Endoscopic Laser Incision for Benign Biliary Strictures: Prospective Evaluation of Safety and Efficacy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 10, 2022 (Anticipated)
Primary Completion Date
October 10, 2025 (Anticipated)
Study Completion Date
October 10, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
Boston Scientific Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is being done to evaluate the safety and efficacy of Percutaneous transhepatic cholangioscopic (PTCS) laser incision as an ancillary therapy to traditional approaches such as balloon dilation and large drain placement for Benign Biliary Strictures (BBS). Narrowing or blockage of the bile ducts (biliary stricture) is a difficult to treat medical condition that leads to life-threatening complications. Treatment usually involves multiple procedures or surgeries spanned over months or years, and in many cases, leads to the need for a life-long tube that drains bile fluid outside of the body and into a bag. PTCS laser incision is a promising new treatment for bile duct strictures. The procedure is performed by an Interventional Radiologist who uses a tiny camera (endoscope) and a laser through a small hole in the skin to open up the blocked or narrowed duct. This allows bile to flow freely where it is supposed to go (without a tube) so that it does not backup up and cause life-threatening problems. Based on early experience from patients who have had this procedure done, it appears to be safe and effective, and may lead to needing fewer procedures over time, with the possibility of living without a tube or drain. The main goal of this study is to confirm the safety and efficacy of PTCS laser incision in a series of patients with benign biliary strictures who would otherwise receive standard treatment with long-term biliary tube drainage.
Detailed Description
PTCS-guided holmium laser incision is a promising new adjuvant treatment for benign biliary strictures. Real-time monitoring under direct endoscopic visualization provides an invaluable opportunity for Interventional Radiologists to safely perform targeted diagnosis and treatment within the biliary system. Despite limited literature on the subject, there are several potential advantages of bringing cholangioscopic laser incision to the Interventional Radiology (IR) suite. First, management of biliary strictures and their sequelae is commonplace in daily IR practice. With increasing sophistication of modern therapeutics including ablation, lithotripter, stent and retrieval devices, there is increasing risk to using fluoroscopy alone to perform complex interventions in a three-dimensional space. Endoscopy allows real-time monitoring of treatment progress and potential complications. For example, an operator using fluoroscopy could not identify iatrogenic haemobilia as readily as an operator using endoscopy, and delayed recognition of such a complication could have lethal consequences. Fortunately, hemorrhagic complications encountered in the IR suite can be treated by trans-arterial embolization. Endoscopic visualization also allows an operator to more precisely characterize the etiology, extent, and other specific features of a focal narrowing within the bile ducts, thus facilitating a more targeted and patient-specific approach to diagnosis and treatment. Conversely, a filling defect seen on conventional cholangiography is nonspecific and can result in an indeterminant biopsy or lead to inappropriate treatment. Second, PTCS-guided laser incision can improve clinical outcomes and potentially be a definitive treatment option for patients with recalcitrant BBS who otherwise require life-long percutaneous drainage. Unlike mechanical dilation techniques such as balloon cholangioplasty and stenting, the holmium laser addresses the root cause of stricture by incising excess fibrotic intraluminal tissue and restoring patency to the native bile duct, while also eliminating the need for an indwelling device that can become a nidus for infection. In contrast to radiofrequency (RF) ablation or the neodymium laser, the holmium laser's short depth of penetration and selective wavelength for water absorption results in precise tissue dissection by way of vaporization, with minimal thermal damage to surrounding tissues. This results in less inflammation and trauma to the bile ducts, which are the major culprits of re-stenosis. Additionally, the device can be employed simultaneously for lithotripsy of concomitant biliary stones which must be removed at the time of intervention to prevent cholangitis and stricture recurrence. Third, PTCS-guided laser incision has the potential to reduce patient morbidity and improve quality of life. By decreasing the total number of interventions and amount of time patients require a drainage catheter or other indwelling device, a decrease in cumulative procedural and stricture-related complications would likewise be expected. In contrast to 1 or 2 PTCS sessions, standard protocols involve multiple interventions over the course of several months, during which time patients are expected to self-manage a biliary drainage bag and continuously monitor for signs and symptoms of cholangitis and elevated bilirubin. Following a capping trial, still some 20-30% of patients develop recurrent stricture, many of whom have no other option but to continue indefinitely with a drainage tube while carrying a life-long risk of recurrent cholangitis and other obstructive phenomena. The improved efficiency of PTCS-guided laser incision also implicates a potential to decrease procedure-related costs, use of hospital and departmental resources, and radiation exposure to patients. In the past, the high overhead cost of reusable endoscopes prohibited most IR groups from adopting endoscopy. However, the development of new disposable low-profile devices has eliminated the financial barrier to entry for IR-operated endoscopy and may yield cost savings over time with less angiography suite usage.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Biliary Strictures With Current or Prior Biliary Obstruction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patients with benign biliary strictures
Arm Type
Other
Arm Description
Patients with benign biliary strictures with current or prior biliary obstruction, who would otherwise receive standard treatment with long-term biliary tube drainage.
Intervention Type
Procedure
Intervention Name(s)
Percutaneous transhepatic cholangioscopic (PTCS) laser incision
Intervention Description
Infrared percutaneous transhepatic cholangioscopic guided holmium laser incision for treatment of benign biliary strictures.
Primary Outcome Measure Information:
Title
Incidence of Post Procedure Adverse Events
Description
Safety evaluated by cumulative rates of post-interventional complications after PTCS-guided laser incision. Complications will be reported according to the Society of Interventional Radiology Adverse Event (AE) classification system. Safety will be reported as 30-day composite of all post-procedure AEs. Complications will be further qualified and quantified by AE severity category and individual AE types.
Time Frame
Up to 24 months
Title
Feasibility of Procedure
Description
Feasibility evaluated by technical success of PTCS-guided laser incision. a. Technical success defined as endoscopic and cholangiographic evidence of improved patency at the time of intervention.
Time Frame
Up to 24 months
Secondary Outcome Measure Information:
Title
Primary Bile Duct Patency
Description
Primary bile duct patency evaluated as mean time to first stricture recurrence. Stricture recurrence will be defined as clinical and/or radiographic evidence of biliary occlusion requiring additional therapy. The date of PTCS or post-intervention biliary catheter removal will mark the time of initiation.
Time Frame
Up to 24 months
Title
Tube-Free Survival
Description
Tube-free survival evaluated as cumulative time survived without a biliary device during the study period. Duration of time that patients require a biliary catheter or stent during follow-up period will be subtracted from the 12-month total. If a device is subsequently removed, tube-free survival time will continue to be accrued up to 12 months post-treatment.
Time Frame
Up to 12 months
Title
12-Month Cumulative Complications
Description
12-month cumulative complications from laser treatment or recurrent biliary disease. a. Composite of all PTCS- and stricture-related AEs during the 12-month follow-up period.
Time Frame
Up to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a diagnosis of Benign Biliary Strictures (BBS) Clinical and/or laboratory evidence of biliary obstruction (current or prior) Age 18 years or older at the time of intervention Exclusion Criteria: Patients with a diagnosis of malignant biliary stricture at the time of enrollment Patients who are subsequently diagnosed with malignant biliary stricture during the study period Liver transplantation within the last 90 days Active cholangitis or sepsis Emergent need for biliary decompression Patients with a diagnosis of primary sclerosing cholangitis with presence of 3 or more strictured segments Patients with a life-expectancy of less than 36 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aniket Joglekar, MD
Phone
310-948-8026
Email
ajoglekar@mednet.ucla.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ravi N Srinivasa, MD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aniket Joglekar, MD
Phone
310-948-8026
Email
ajoglekar@mednet.ucla.edu

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Percutaneous Endoluminal Benign Biliary Laser

We'll reach out to this number within 24 hrs