- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05746832
Failed Retrograde Cholangiopancreatography (ERCP) Stone Extraction: Surgical Interference
January 29, 2024 updated by: Zyad Osama Harith, Assiut University
Failed Retrograde Cholangiopancreatography (ERCP) Stone Extraction: Surgical Interference Versus Follow up on Stent.
Assessment of the differences in stone size and the largest CBD diameter before and after stenting in one or two sessions.
Stone clearance and complications were also determined with the ERCP, and factors associated with complete clearance were evaluated in patients with difficult CBD stones (a large [≥ 20 mm] or multiple [≥ 3 sized ≥ 15 mm] CBD stones).
And also compared the outcomes with conventional procedure of open surgery.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Gallstones are a very common problem in developed countries.
Most patients with gallstones remain asymptomatic throughout their lifetime, but 10 % - 25 % of them may develop biliary pain or complications, with an annual risk of about 2 % - 3 % for symptomatic disease and 1 % - 2 % for major complications.
The development of symptomatic disease and complications is mostly related to the migration of stones into the common bile duct (CBD).
Common bile duct stones (CBDSs) may be treated by endoscopic retrograde cholangiopancreatography (ERCP) or surgically during cholecystectomy.
Removal of common bile duct (CBD) stones can still be difficult in patients with large or multiple stones despite an adequate sphincterotomy.
Procedures such as mechanical, extracorporeal, electrohydraulic or laser lithotripsy, and chemical dissolution have been introduced as effective therapeutic interventions for irretrievable CBD stones.
However, these techniques have their drawbacks, are not widely available, or are still under clinical evaluation.
Several studies have shown that insertion of an endoscopic biliary stent is a safe, effective, and widely available measure.
An indwelling stent provides biliary drainage and fragments large stones, thereby reducing the risk of cholangitis and allowing stones to pass spontaneously or rendering them more extractable at a later procedure.
Thus, this study intends to shed a light on advances in diagnosis and management in patients with biliary difficult stones.
Study Type
Interventional
Enrollment (Estimated)
3
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Zyad Osama Harith, resident
- Phone Number: 01149863511
- Email: zyadosama200000@gmail.com
Study Contact Backup
- Name: Mostafa Mahmoud Mohammed Sayed, ass prof
- Phone Number: +201271207839
- Email: mostafa.sayed@aun.edu.eg
Study Locations
-
-
-
Assiut, Egypt, 71515
- Assiut universty Hospital
-
-
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
15 years to 80 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- All cases of difficult common bile duct stones leading to variable occlusion.
- Patients fit for intervention.
- Patients informed consent for study.
Exclusion Criteria:
- Surgically unfit cases according to ASA
- Locally advanced irresectable cases.
- Patients refuse consent to participate in the study.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: One session application of (ERCP) in the management of common bile duct stones.
One session application of endoscopic stenting retrograde cholangiopancreatography (ERCP) in the management and clearance of difficult common bile duct stones and assessment of the differences in stone size and the largest CBD diameter before and after stenting in one or two sessions.
Stone clearance and complications were also determined with the ERCP, and factors associated with complete clearance were evaluated in patients with difficult CBD stones (a large [≥ 20 mm] or multiple [≥ 3 sized ≥ 15 mm] CBD stones).
And also compared the outcomes with conventional procedure of open surgery.
|
Assessment of the differences in stone size and the largest CBD diameter before and after stenting in one or two sessions.
Stone clearance and complications were also determined with the ERCP, and factors associated with complete clearance were evaluated in patients with difficult CBD stones (a large [≥ 20 mm] or multiple [≥ 3 sized ≥ 15 mm] CBD stones).
And also compared the outcomes with conventional procedure of open surgery.
|
|
Active Comparator: Two sessions application of (ERCP) in the management of common bile duct stones.
Two sessions application of endoscopic stenting retrograde cholangiopancreatography (ERCP) in the management and clearance of difficult common bile duct stones.and
assessment of the differences in stone size and the largest CBD diameter before and after stenting in one or two sessions.
Stone clearance and complications were also determined with the ERCP, and factors associated with complete clearance were evaluated in patients with difficult CBD stones (a large [≥ 20 mm] or multiple [≥ 3 sized ≥ 15 mm] CBD stones).
And also compared the outcomes with conventional procedure of open surgery.
|
Assessment of the differences in stone size and the largest CBD diameter before and after stenting in one or two sessions.
Stone clearance and complications were also determined with the ERCP, and factors associated with complete clearance were evaluated in patients with difficult CBD stones (a large [≥ 20 mm] or multiple [≥ 3 sized ≥ 15 mm] CBD stones).
And also compared the outcomes with conventional procedure of open surgery.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time of procedure.
Time Frame: On the day of determined procedure.
|
This is measured in hours.
|
On the day of determined procedure.
|
|
Rate of stone size reduction.
Time Frame: Baseline.
|
This is measured in millimeters.
|
Baseline.
|
|
Width of CBD.
Time Frame: Baseline.
|
This is measured in millimeters.
|
Baseline.
|
|
Degree of stone clearance and complications.
Time Frame: Baseline.
|
Those are determined by close monitoring of patients whether after ERCP or surgery.
|
Baseline.
|
|
Postoperative morbidity and mortality.
Time Frame: Baseline.
|
Those are measures in percentage of patients in the study.
|
Baseline.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood loss during the procedure.
Time Frame: Baseline.
|
This is measured in milliliters.
|
Baseline.
|
|
Postoperative wound infection.
Time Frame: Baseline.
|
This is measured in percentage of patients in the study.
|
Baseline.
|
|
Postoperative hospital stay.
Time Frame: Baseline.
|
This is measured in days.
|
Baseline.
|
|
Postoperative hemorrhage.
Time Frame: Baseline.
|
This is measured in milliliters.
|
Baseline.
|
|
Postoperative 30 day mortality rate.
Time Frame: Baseline.
|
This is measured in percentage of patients in the study.
|
Baseline.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hisham Ali Ryad, Prof., Assiut university
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 (Estimated)
September 1, 2024
Primary Completion (Estimated)
December 1, 2024
Study Completion (Estimated)
December 1, 2024
Study Registration Dates
First Submitted
November 1, 2021
First Submitted That Met QC Criteria
February 23, 2023
First Posted (Actual)
February 28, 2023
Study Record Updates
Last Update Posted (Actual)
January 31, 2024
Last Update Submitted That Met QC Criteria
January 29, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CBD stones managment by ERCP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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