Skip to content

Clinical study of ICG fluorescence-guided partial hepatectomy for resectable hepatocellular carcinoma

Clinical study of ICG fluorescence-guided partial hepatectomy for resectable hepatocellular carcinoma

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103578
Enrollment
Unknown
Registered
2025-05-30
Start date
2024-07-23
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Liver cancer

Interventions

Surgical modalities Group A:ICG fluorescence-guided partial hepatectomy
Surgical modalities Group B:Anatomic partial hepatectomy

Sponsors

the first affiliated hospital of Chongqing medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Patients with hepatocellular carcinoma who underwent pathology or abdominal enhanced CT/MRI and met the definition of primary liver cancer diagnosis and treatment standard of China 2022 edition; 2 Measurable lesions that meet the RECIST criteria; 3 Resectable defined as primary liver cancer of CNLC stage Ia, Ib, or IIa with good liver reserve function, and the tumor is not located in the central part of the liver and far away from large blood vessels, bile ducts, hepatic hilar and other unresectable areas. Other physical conditions: patients are assessed to have general safety conditions for surgery, including good cardiopulmonary function, no serious comorbidities and no contraindications. 4 Previously untreated patients; 5 Liver function Child-Pugh grade A and Eastern Cooperative Oncology Group Physical Status Activity (ECOGPS) score <2; 6 Informed understanding of all treatment options and good compliance with outpatient follow-up, with complete follow-up data.

Exclusion criteria

Exclusion criteria: 1 Patients with combined organic lesions of important organs such as heart, brain and kidney or accompanied by other malignant tumors; 2 Patients with other treatment modalities of previous previous hepatocellular carcinoma; 3 Liver function failure (liver function Child-Pugh classification B/C); 4 Patients with incomplete clinical data; 5 Patients with poor compliance, pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Overall survival (OS) for both surgical modalities;Surgical time in patients with both surgical modalities;disease-free survival (DFS) for both surgical modalities;bleeding in patients with both surgical modalities;

Secondary

MeasureTime frame
Liver and kidney function;complication;blood routine;coagulation function;tumor markers;

Countries

China

Contacts

Public ContactDu Chengyou

the first affiliated hospital of Chongqing medical university

lanxiangkeyan@163.com+86 136 2978 0427

Outcome results

None listed

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