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Safety and feasibility of laparoscopic hemihepatectomy assisted by real-time surgical navigation technology: a single-center, single-blind, randomized controlled clinical trial

Safety and feasibility of laparoscopic hemihepatectomy assisted by real-time surgical navigation technology: a single-center, single-blind, randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112678
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Hepatocellular carcinoma

Interventions

Navigation group:A surgical navigation system was used to perform laparoscopic hemihepatectomy.
Non-navigation group:Conventional laparoscopic hemihepatectomy was performed without the use of surgical navigation system.

Sponsors

Shenzhen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age of 18-75 years old, both sexes; 2. Imaging and preoperative evaluation confirmed liver occupying lesions (suspected liver tumor), and laparoscopic hemihepatectomy was planned; 3.Preoperative liver function Child-Pugh A or B, ICG R15 <= 15%; 4. ECOG score 0-1; 5. The indications for laparoscopic surgery were evaluated by the multidisciplinary team and the department before surgery; 6. Those who volunteered to participate in the study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiopulmonary dysfunction or other important organ dysfunction, unable to tolerate surgery; 2. Distant metastasis or extensive peritoneal dissemination; 3.Previous history of major upper abdominal surgery leading to severe adhesion affecting the laparoscopic operator; 4. Pregnant or lactating women; Inability to cooperate with the investigator due to mental or cognitive impairment; 5. The planned plan could not be completed because of tumor invasion or other reasons to expand the scope of surgical resection during operation.

Design outcomes

Primary

MeasureTime frame
Intraoperative blood loss per unit liver resection area;

Countries

China

Contacts

Public ContactLiping Liu

Shenzhen People's Hospital

liuliping@mail.sustech.edu.cn+86 755 2294 8140

Outcome results

None listed

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