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Prospective, multicenter, randomized, controlled clinical study of regional lymphotomy and extended lymphotomy in hilar cholangiocarcinoma

Prospective, multicenter, randomized, controlled clinical study of regional lymphotomy and extended lymphotomy in hilar cholangiocarcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015688
Enrollment
Unknown
Registered
2018-04-15
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

hilar cholangiocarcinoma

Interventions

1:Regional resection of hilar cholangiocarcinoma (8a/p, 12a/b/c/h/p, 13a).
2:Hilar cholangiocarcinoma resection and extended lymph node dissection (8a/p, 9,12a/b/c/h/p, 13a, 14, 16).

Sponsors

Renji Hospital Affiliated to Medical School, Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) patients aged 18 to 80 years old; 2) diagnosis of hilar cholangiocarcinoma (imaging, laboratory examination, intraoperative frozen, postoperative pathological diagnosis of cholangiocarcinoma; 3) the tumor can be removed completely; 4) the patient is autonomous, understands and voluntarily signs written informed consent and is able to complete the follow-up plan; 5) pregnant women should be excluded from pregnancy; 6) Child-Turcotte-Pugh score of liver function A-B, the upper limit of serum bilirubin = normal value is 1.5 times and the upper limit of alt AST = normal value is 2 times; Anhydride clearance = 60ml / min, hemoglobin = 90g / L; ASA 1-4; 7) sign written informed consent before screening.

Exclusion criteria

Exclusion criteria: 1) resection of tumor R1; 2) the patients had significant heart, lung, brain and renal dysfunction affecting the management of cholangiocarcinoma; 3) the patient has other malignant tumor history; 4) Child-Turcotte-Pugh grade C of liver function; 5) Women who are pregnant or are breastfeeding; 6) the researcher decided that he was not fit to participate in this study.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactJian Wang

Renji Hospital Affiliated to Medical School, Shanghai Jiaotong University

shirley0815@126.com+86 13917019110

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 2, 2026