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Clinical application of laparoscopy combined with choledochoscopy in the treatment of complex intrahepatic and extrahepatic bile duct stones

Clinical application of laparoscopy combined with choledochoscopy in the treatment of complex intrahepatic and extrahepatic bile duct stones

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077631
Enrollment
Unknown
Registered
2023-11-14
Start date
2023-11-15
Completion date
Unknown
Last updated
2023-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Complex intrahepatic and extrahepatic bile duct stones

Interventions

Laparoscopic left hemihepatectomy with left hepatic duct stump anterograde common bile duct exploration and stone removal group (experimental group):None
Partial hepatectomy with common bile duct exploration and T-tube drainage group:None

Sponsors

Central Theater Command General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Participants aged 18 to 90 years old; 2. Participants who underwent preoperative abdominal ultrasound, abdominal CT, and abdominal MRCP to confirm the presence of left lobe bile duct stones with common bile duct stones or a small amount of stones in the right lobe, as well as atrophy of the left lobe liver parenchyma; 3. Liver function grading (Child Pugh grading) A or B, liver function reserve test ICG15<10%.

Exclusion criteria

Exclusion criteria: 1. Pregnant woman; 2. With a history of major abdominal surgery; 3. Combined with malignant tumors (including intrahepatic and extrahepatic cholangiocarcinoma) or hematological diseases.

Design outcomes

Primary

MeasureTime frame
routine blood test;liver function;coagulation;Intraoperative bleeding volume;operative time;Pain score;Extubation time;

Countries

China

Contacts

Public Contactyilin hu

Central Theater Command General Hospital

yilin_hu@163.com+86 133 9605 8828

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026