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The establishment of hemostatic procedures subsequent to hepatectomy under the IDEAL framework: a phase I, validatory trial

The establishment of hemostatic procedures subsequent to hepatectomy under the IDEAL framework: a phase I, validatory trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088630
Enrollment
Unknown
Registered
2024-08-22
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Carcinoma, Hepatocellular

Interventions

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 75 years; no gender restriction; 2. Newly diagnosed and untreated liver mass, whether benign or malignant; 3. Proposed open or laparoscopic hepatectomy with anticipated hepatic resection of >=3 segments(large hepatectomy) ; 4. Sufficient residual liver volume, with residual liver volume in cirrhotic patients accounting for more than 40% of standard liver volume, and in non-cirrhotic patients accounting for more than 30% of standard liver volume; 5. Good liver function and hepatic reserve: Child-Pugh grade A; ICGR 15 < 20%; 6. Good hematologic and major organ function.

Exclusion criteria

Exclusion criteria: 1. Combined with hematologic disorders that adversely affect coagulation function; 2. Human immunodeficiency virus (HIV) infection, or suffering from autoimmune diseases; 3. Currently participating in another clinical study; 4. Other factors that may affect the study results or cause the study to be terminated prematurely, as judged by the investigator.

Design outcomes

Primary

MeasureTime frame
Surface-related complication after hepatectomy;

Secondary

MeasureTime frame
The volume of drainage fluid during the initial three days after surgery;The bilirubin concentration of drainage fluid during the initial three days after surgery;The haemoglobin concentration of drainage fluid during the initial three days after surgery;Fluid volume in the surgical area at 1 week after surgery;Pleural effusion at 1 week after surgery;Other complications after surgery;

Countries

China

Contacts

Public ContactWei Peng

West China Hospital, Sichuan University

pengwei@wchscu.cn+86 150 0286 6735

Outcome results

None listed

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