- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02592811
Comparison of Endoscopic Sphincterotomy Plus Large-balloon Dilatation and Conventional Treatment for Large CBD Stones
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
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Phase 3
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
|
Common bile duct cannulation with a cannulation catheter
Other Names:
Endoscopic large sphincterotomy
Other Names:
Large Balloon Dilatation : with the HERCULES, Cook 12, 15, 18 or 20 mm of diameter (adapted to stone diameter)
Other Names:
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)
|
Common bile duct cannulation with a cannulation catheter
Other Names:
Endoscopic large sphincterotomy
Other Names:
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 :
|
1 month
|
|
Number of patients with mild or severe ACUTE PANCREATITIS (Morbidity) after ERCP
Time Frame: 1 month
|
Immediate complications were noted :
|
1 month
|
|
Number of patients with PERFORATION (Morbidity of ERCP)
Time Frame: 1 day
|
|
1 day
|
|
Number of patients with post ERCP INFECTION as angiocholitis, cholecystitis or urine infection, septicemia (Morbidity of ERCP)
Time Frame: 1 month
|
|
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
|
|
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
Investigators
- Principal Investigator: David KARSENTI, MD, Société Française d'Endoscopie Digestive
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SocieteFranceED
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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