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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05901363
Other study ID # SVU/MED/SUR011/4/23/4/613
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2019
Est. completion date October 30, 2022

Study information

Verified date June 2023
Source South Valley University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Around 10-18% of patients undergoing cholecystectomy for gallstones have common bile duct (CBD) stones. Currently, various procedures for the treatment of cholecystocholedocholithiasis are available including open cholecystectomy plus open common bile duct exploration (OC+OCBDE), laparoscopic cholecystectomy plus laparoscopic common bile duct exploration (LC+LCBDE), may be trans-cystic or trans-choledochal, and laparoscopic cholecystectomy plus endoscopic retrograde cholangiopancreatography (LC+ERCP), which may be performed pre, at, or after LC.


Description:

Around 10-18% of patients undergoing cholecystectomy for gallstones have common bile duct (CBD) stones. Currently, various procedures for the treatment of cholecystocholedocholithiasis are available including open cholecystectomy plus open common bile duct exploration (OC+OCBDE), laparoscopic cholecystectomy plus laparoscopic common bile duct exploration (LC+LCBDE), may be trans-cystic or trans-choledochal, and laparoscopic cholecystectomy plus endoscopic retrograde cholangiopancreatography (LC+ERCP), which may be performed pre, at, or after LC. Single-session treatment of gallbladder and CBD stones is safe, efficient, shortens hospital stay, and is less expensive than staged procedures. Although there is some evidence suggesting that LCBDE may be associated with a lower rate of retained stones compared with ERCP, previous studies comparing LCBDE with ERCP and stone extraction have collectively failed to demonstrate the superiority of one approach over the other.


Recruitment information / eligibility

Status Completed
Enrollment 218
Est. completion date October 30, 2022
Est. primary completion date October 30, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: 1. Patients diagnosed with cholecystocholedocholithiasis 2. American Society of Anesthesiologists (ASA) scores of I-III 3. Age 20-70 years. Exclusion Criteria: 1. cholangitis, 2. acute biliary pancreatitis, 3. suspected Mirizzi syndrome, 4. suspected hepatobiliary malignancy, 5. perforated gallbladder, 6. biliary peritonitis, 7. intrahepatic stones, 8. pregnancy, 9. previous cholecystectomy, 10. altered anatomy such as Billroth II reconstruction or any form of Roux-en-Y reconstruction that interfere with the endoscopic approach, 11. Contraindications to laparoscopic surgery as severe liver cirrhosis or upper abdominal surgery were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Endoscopic retrograde cholangiopancreatography plus laparoscopic cholecystectomy
laparoscopic removal of gallbladder and endoscopic extraction of common bile duct stones
aparoscopic common bile duct exploration and laparoscopic cholecystectomy
laparoscopic removal of gallbladder and laparoscopic extraction of common bile duct stones

Locations

Country Name City State
Egypt Mohammed Ahmed Omar Qina Qena

Sponsors (1)

Lead Sponsor Collaborator
South Valley University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary success rate successful laparoscopic cholecystectomy and successful common bile duct stone extraction 2 years
Secondary operative time the overall time of the procedure from 1 to 5 hours
Secondary morbidity any intraoperative or postoperative adverse event 3 years
Secondary mortality death of patient 3 years
Secondary Hospital stay the length of hospital stay from the day of admission to the day of discharge 30 days
Secondary the number of hospital readmission 3 years
Secondary the number of postoperative intervention 3 years
Secondary The total cost of treatment 30 days
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