Status:

COMPLETED

Non-Complex Biliary Stones DSC vs ERC

Lead Sponsor:

Boston Scientific Corporation

Conditions:

Biliary Stones

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

To prospectively compare non-complex biliary stone clearance using fluoroscopy/radiation-free direct solitary cholangioscopy (DSC) utilizing the SpyGlass™ system with non-complex biliary stone clearan...

Detailed Description

The objective of this study is to prospectively compare non-complex biliary stone clearance using fluoroscopy/radiation-free direct solitary cholangioscopy (DSC) utilizing the SpyGlass™ system with no...

Eligibility Criteria

Inclusion

  • 18 years or older
  • Abdominal pain consistent with choledocholithiasis (procedure possible within 72 hours of onset of symptoms and imaging suggesting choledocholithiasis, contingent on persistent abdominal pain)
  • Abnormal LFTs
  • Non-complex biliary stone disease, defined as 5 or fewer stones in the common bile or common hepatic duct with largest stone no larger than 10 mm in size. If stones not seen on imaging (US, CT) the bile duct diameter should be ≤12 mm\*
  • \* Given the poor sensitivity (approximately 20%) for biliary stones of CT and US, the diameter of the dilated CBD is used as a surrogate for largest stone diameter
  • Availability of non-invasive imaging to determine the diameter of the bile duct and number and size of bile duct stones if visible on imaging
  • If probability of stones is high per investigator assessment based on ASGE criteria, any standard of practice imaging modality (eg. abdominal US) is acceptable.
  • If the probability of stones is either intermediate or low per investigator assessment based on ASGE criteria, MRCP or EUS imaging is required to confirm presence of stones.
  • Willing and able to comply with the study procedures and provide written informed consent to participate in the study

Exclusion

  • Potentially vulnerable subjects, including but not limited to pregnant women and subjects in whom an endoscopic procedure is contraindicated
  • Location of the stones in intrahepatic ducts, cystic duct or proximal to strictures
  • Bile duct stricture noted distal to stone on MRCP, which would make extraction without lithotripsy impossible
  • Ongoing cholangitis at time of randomization, manifested by fever with tachycardia and hypotension or evidence of pus at the ampulla
  • Patients with prior biliary sphincterotomy
  • Patients with Primary Sclerosing Cholangitis (PSC)
  • Acute pancreatitis, defined as abdominal pain and serum concentration of pancreatic enzymes \[lipase (required), amylase (optional)\] three or more times the upper limit of normal
  • Surgically altered gastro-duodenal luminal anatomy other than prior Billroth I reconstruction, as these would be anticipated to lead to more complicated procedures
  • Coagulopathy or ongoing need for anti-coagulation

Key Trial Info

Start Date :

September 21 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 8 2023

Estimated Enrollment :

250 Patients enrolled

Trial Details

Trial ID

NCT03421340

Start Date

September 21 2018

End Date

October 8 2023

Last Update

January 17 2025

Active Locations (8)

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Page 1 of 2 (8 locations)

1

Stanford University Medical Center

Stanford, California, United States, 94305

2

University of Colorado Hospital, Denver

Aurora, Colorado, United States, 80045

3

Ochsner Clinic Foundation

New Orleans, Louisiana, United States, 70121

4

Ertan Digestive Disease Center - University of Texas Health Science Center

Houston, Texas, United States, 77030