Comparison of Endoscopic Sphincterotomy Plus Large-balloon Dilatation and Conventional Treatment for Large CBD Stones

October 28, 2015 updated by: KARSENTI, Société Française d'Endoscopie Digestive

Endoscopic Sphincterotomy Plus Large-Balloon Dilatation (ESLBD) Versus Conventional Endoscopic Treatment for Removal of Large Common Bile Duct Stones : A Prospective Comparative Multi Center Randomized Study

Bile duct stone extraction is impossible after endoscopic sphincterotomy (ES) alone in approximatively 10% of cases (mostly because of stones' size). Adjunction of a mechanical lithotripsy (ML) is well established to improve clearance of common bile duct (CBD) stones. Because of inconstant success, high cost, and length of procedure, an alternative method was proposed in 2003: endoscopic sphincterotomy plus large balloon dilatation (ESLBD). If the safety of ESLBD is accepted in all recent published studies, it remains controversial wether ESLBD is superior to conventional endoscopic treatment associating ES± ML for CBD stones. Procedure treatment and place of ESLBD in CBD stones therapeutic strategy is unclear.

The purpose of this prospective comparative multi center randomized study is to evaluate the superiority or not of ESLBD on conventional treatment (ES±ML) for the treatment of large bile duct stone (≥13mm) after standard ES, and to propose a new CBD stones therapeutic strategy.

Study Overview

Study Type

Interventional

Enrollment (Actual)

150

Phase

  • Phase 3

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patient with CBD stones with a smaller diameter ≥ 13mm on cholangiogram

Exclusion Criteria:

  • Active or history of acute pancreatitis
  • Presence of intrahepatic stones
  • History of Billroth II or roux-en-Y reconstruction
  • Coagulation disorder (partial thromboplastin time > 42 seconds, prothrombin time (Quick value) < 50% and platelet count of <50 000/mm3)
  • Current anticoagulation or clopidogrel treatment
  • Pregnancy
  • Inability to give informed consent

Study Plan

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

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: ESLBD

Endoscopic Sphincterotomy plus Large Balloon Dilatation +/- lithotripsy

  1. ERCP with deep cancellation of BDS
  2. Endoscopic large sphincterotomy
  3. Large Balloon Dilatation of Oddi Sphincter: with the HERCULES, Cook 12, 15, 18 or 20 mm of diameter (adapted to stone diameter)
  4. Stone extraction with dormia basket or extraction balloon
  5. Mechanical Lithotripsy if needed
Common bile duct cannulation with a cannulation catheter
Other Names:
  • Cholangiogram with deep cannulation of CBD
Endoscopic large sphincterotomy
Other Names:
  • ES
Large Balloon Dilatation : with the HERCULES, Cook 12, 15, 18 or 20 mm of diameter (adapted to stone diameter)
Other Names:
  • LBD, LBDS
After dilatation, extraction of stones is done with dormia basket or extraction balloon and if not possible a mechanical lithotripsy is performed
Active Comparator: CONV

Conventional treatment associating Endoscopic Sphincterotomy +/- Mechanical Lithotripsy (ES+/-LM)

  1. ERCP with deep cancellation of BDS
  2. Endoscopic large sphincterotomy
  3. Stone extraction with dormia basket or extraction balloon
  4. Mechanical Lithotripsy if needed
Common bile duct cannulation with a cannulation catheter
Other Names:
  • Cholangiogram with deep cannulation of CBD
Endoscopic large sphincterotomy
Other Names:
  • ES
After dilatation, extraction of stones is done with dormia basket or extraction balloon and if not possible a mechanical lithotripsy is performed

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Success of common bile duct clearance in one session of ERCP (endoscopic retrograde cholangiopancreatography)
Time Frame: 1 month
1 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of patients with mild or severe BLEEDING (Morbidity) after ERCP
Time Frame: 1 month

Immediate complications were noted :

  • bleeding : mild if blood transfusion not necessary, and severe if blood transfusion necessary
  • Clinical data (pain, fever, vomiting...) are noted during first month
  • Clinical examination and blood tests (Blood count, C reactive protein, lipase blood test, hepatic tests, creatininemia) were noted at the 30th day after procedure
  • In case of bleeding suspected, a new ERCP was done
  • Number of patients with bleeding and with any complication in both groups were noted and compared
1 month
Number of patients with mild or severe ACUTE PANCREATITIS (Morbidity) after ERCP
Time Frame: 1 month

Immediate complications were noted :

  • Acute pancreatitis : defined by the association of abdominal pain and lipase blood test > 3 N
  • Severity of acute pancreatitis was evaluated on CT index, and on evolution data
  • Clinical data (pain, fever, vomiting...) are noted during first month
  • Clinical examination and blood tests (Blood count, C reactive protein, lipase blood test, hepatic tests, creatininemia) were noted at the 30th day after procedure
  • Abdominal CT was performed in case of suspected acute pancreatitis
  • Number of patients with Acute Pancreatitis and any complication in both groups were noted and compared
1 month
Number of patients with PERFORATION (Morbidity of ERCP)
Time Frame: 1 day
  • Suspected on clinical data (pain, fever, vomiting...) and blood tests (Blood count, C reactive protein) noted during first day after ERCP:
  • confirmed on CT
  • Number of patients with perforation in both groups were noted and compared, and global morbidity in both groups were noted and compared
1 day
Number of patients with post ERCP INFECTION as angiocholitis, cholecystitis or urine infection, septicemia (Morbidity of ERCP)
Time Frame: 1 month
  • Suspected on clinical data (pain, fever, vomiting...), blood tests (Blood count, C reactive protein, blood and urine cultures), noted during first day after ERCP, during 30th day and more if necessary in the meantime
  • Abdominal US and CT were performed if necessary
  • Number of patients with infection in both groups were noted and compared, and global morbidity in both groups were noted and compared
1 month
GLOBAL MORBIDITY of ERCP (number of patients with bleeding and/or acute pancreatistis and/or perforation and/or infection)
Time Frame: 1 month
- Number of patients with any complication as bleeding, acute pancreatitis, perforation, infection (as angiocholitis, cholecystitis, urine infection or septicemia) happened in both groups during the first month after the procedure were noted and compared
1 month
MORTALITY of ERCP
Time Frame: 1 month
- Number of death happened in both groups during the first month after the procedure were noted and compared
1 month
Number of patients with recurrence of BDS
Time Frame: 1 month
  • Clinical data (pain, fever, vomiting...) are noted during first month
  • Clinical examination and blood tests (Blood count, C reactive protein, lipase blood test, hepatic tests, creatininemia) were noted at the 30th day after procedure
  • In case of recurrence BDS suspected, abdominal US and/or CT and/or MRI and/or EUS (Endoscopic Ultrasonography) were done, and if BDS was confirmed, a new ERCP was done
  • Number of patients with recurrence of BDS in both groups in the first month after the procedure were noted and compared
1 month
Length of procedure
Time Frame: Day one
For each patient, time was noted at the beginning and at the end of ERCP
Day one
Cost of procedure
Time Frame: Day one
All the instrument used during ERCP (endoscopic retrograde cholangiopancreatography) for each patient were noted, and at the end of procedure cost of all instruments were recorded
Day one
comparison of the frequency of mechanical lithotripsy of both groups
Time Frame: Day one
In both groups mechanical lithotripsy can be performed in case of impossibility of stone extraction. The rate of lithotripsy performed in both groups were compared
Day one

Collaborators and Investigators

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

Investigators

  • Principal Investigator: David KARSENTI, MD, Société Française d'Endoscopie Digestive

Publications and helpful links

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

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 Major Dates

Study Start

July 1, 2010

Primary Completion (Actual)

March 1, 2015

Study Completion (Actual)

March 1, 2015

Study Registration Dates

First Submitted

October 5, 2015

First Submitted That Met QC Criteria

October 28, 2015

First Posted (Estimate)

October 30, 2015

Study Record Updates

Last Update Posted (Estimate)

October 30, 2015

Last Update Submitted That Met QC Criteria

October 28, 2015

Last Verified

October 1, 2015

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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