Skip to content

Comparative study between laparoscopic and open distal pancreatectomy for patients with pancreatic cancer: a retrospective and propensity score-matching

Comparative study between laparoscopic and open distal pancreatectomy for patients with pancreatic cancer: a retrospective and propensity score-matching

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000041065
Enrollment
Unknown
Registered
2020-12-17
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-03-01

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

Conditions

Pancreatic cancer

Interventions

Sponsors

The First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients aged 18 to 80 years, regardless of gender; (2) Patients confirmed adenocarcinoma of pancreatic body and tail duct, without distant metastasis.Resectable or borderline resectable pancreatic adenocarcinoma follow 2020 V1 NCCN; (3) Eastern Cooperative Oncology Group (ECOG) performance status 0 to 1; (4) The expected postoperative survival >= 3 months; (5) Follow-up in time and ability to comply with research plans and other program requirements; (6) Volunteer to be the subject and sign the informed consent. (7) Normal hematological index (Leukocyte, platelet, liver function, renal function, DIC, electrolyte index, Hb >10g/dL).

Exclusion criteria

Exclusion criteria: (1) Patients have contraindication to surgery; (2) Patients confirmed locally advanced or unresectable pancreatic cancer (refer to 2020.V1 version of NCCN Pancreatic Cancer Guidelines); (3) Imaging studies found distant metastases; (4) Patients with severe impairment of cardiac, liver or kidney function (Cardiac function grade 3-4, ALT or AST exceeds 5 times the upper limit of normal value, Creatinine exceeds the upper limit of normal); (5) Pregnant or lactating female patients; (6) Patients with other malignant tumors or hematological diseases; (7) Patients have participated in other clinical trials of pancreatic cancer within three months.

Design outcomes

Primary

MeasureTime frame
Overall survival;RFS;

Secondary

MeasureTime frame
Postoperative morbidity;Postoperative hospital stays;Total charge;Operative time;Blood loss;Pain score (VSA);R0 resection rate;30-day mortality or in-hospital mortality;POPF (postoperative pancreatic fistula);

Countries

China

Contacts

Public ContactChunlin Ge

The First Affiliated Hospital of China Medical University

gechunlin@139.com+86 13998303666

Outcome results

None listed

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