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A prospective randomized controlled study of the outcomes of laparoscopy and open surgery after neoadjuvant chemotherapy for pancreatic cancer

A prospective randomized controlled study of the outcomes of laparoscopy and open surgery after neoadjuvant chemotherapy for pancreatic cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029987
Enrollment
Unknown
Registered
2020-02-18
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Pancreatic cancer

Interventions

experimental group:laparoscopic pancreatectomy
control group:open pancreatectomy

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients confirmed resectable or borderline resectable pancreatic adenocarcinoma after neoadjuvant chemotherapy follow 2020 V1 NCCN; 2. Patients aged 18 to 80 years, regardless of gender; 3. Eastern Cooperative Oncology Group (ECOG) performance status 0 to 1; 4. The expected postoperative survival >= 3 months; 5. Ability to comply with research plans and other program requirements; 6. Volunteer to be the subject and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients have contraindication to surgery; 2. Patients confirmed locally advanced or unresectable pancreatic cancer after neoadjuvant chemotherapy (refer to 2020.V1 version of NCCN Pancreatic Cancer Guidelines); 3. Imaging studies found distant metastases; 4. Patients with severe impairment of cardiacliver 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 participanted in other clinical trials of pancreatic cancer within three months.

Design outcomes

Primary

MeasureTime frame
overall survival;

Secondary

MeasureTime frame
disease-free survival;R0 resection rate;operative duration;number of lymph node dissection;major postoperative complications;minor postoperative complications;length of postoperative hospital stay;length of postoperative ICU stay;intraoperative blood loss;90-day mortality;

Countries

China

Contacts

Public ContactBing Peng

West China Hospital of Sichuan University

pengbing84@hotmail.com+86 18980601481

Outcome results

None listed

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