Skip to content

A prospective randomized controlled trial comparing an upper midline incision with a traditional right subcostal oblique incision for resection of a single hepatocellular carcinoma tumor meeting the Milan criteria

A prospective randomized controlled trial comparing an upper midline incision with a traditional right subcostal oblique incision for resection of a single hepatocellular carcinoma tumor meeting the Milan criteria

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13004486
Enrollment
Unknown
Registered
2013-12-15
Start date
2014-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hepatocellular carcinoma

Interventions

a traditional right subcostal oblique incision:Use a traditional right subcostal oblique incision for hepatectomy

Sponsors

Department of Liver Surgery, West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. A single HCC tumor with the diameter of =5cm; 2. Male or Female Aged 18-65 years old; BMI=25; 3. Patients can tolerate hepatectomy and have good live functions with Child-Pugh A; 4. Patients volunteered and signed the informed consent; 5. Patients have not recieved other surgeries; 6. Patient has a good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients who refused to sign the informed consent; 2. Pregnant or lactating women; 3. Patients’vital organs had severe dysfunction and they cannot tolerate surgery; 4. Patient has a bad compliance.

Design outcomes

Primary

MeasureTime frame
tumor related data;operating related data;postoperative related data;related data in the follow-up;degree of satisfaction;survival;tumor recurrence rate;

Countries

China

Contacts

Public ContactLi Jiang

Department of Liver Surgery, West China Hospital of Sichuan University

jl339@126.com+86 13880900287

Outcome results

None listed

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