liver cancer
Conditions
Interventions
Liver suspension device (the experimental group):A laparoscopic hepatectomy simple suspension device is inserted through the Trocar hole. After the needle holder adjusts the needle, the target liver
laparoscopic hepatectomy alone (the control group):Routine laparoscopic hepatectomy
Sponsors
Third Affiliated Hospital of Naval Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1) Be between 18 and 75 years old, regardless of gender; 2) The case data is complete, and the diagnosis is hepatocellular carcinoma (AFP, DCP increase with CT, MRI for diagnosis) 3) The tumor is located in the S1, S4a, S7, S8 segments, and laparoscopic surgery is planned 4) Patients whose tumors are BCLC staged (Barcelona stage) for stage 0-A 5) Preoperative liver function score of Child-pough stage A 6) Good preoperative cardiopulmonary function assessment and able to tolerate surgery 7) Those who can understand the situation of this research and have signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1) Patients who need to open the abdomen due to other surgical procedures 2) Patients who have multiple surgeries and need to spend a lot of time to release abdominal or intestinal adhesions 3) Patients with intraoperative blood loss or abdominal opening caused by non-complicated liver segment resection factors 4) Patients who are forced to undergo emergency surgery due to tumor rupture and bleeding 5) Mental abnormalities 6) Coagulation dysfunction 7) Patients who cannot obtain informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amount of intraoperative bleeding;Intraoperative transfusion rate;Duration of surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative biliary leakage incidence;Surgeon satisfaction; | — |
Countries
China
Contacts
Public ContactXiaoying Zhu
Third Affiliated Hospital of Naval Medical University
Outcome results
None listed