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Robotic Pancreatic Telesurgery Leveraging a 5G and Dedicated Internet Access Platform

Application of Domestic Robotic Systems in Remote Pancreatic Surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108987
Enrollment
Unknown
Registered
2025-09-10
Start date
2025-05-10
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Pancreatic Neoplasms: Benign and Malignant

Interventions

Telesurgery Group:Performance of Robotic Teleoperative Pancreatic Surgery

Sponsors

Chinese People’s Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Obtain informed consent for telesurgical robotic procedures signed by the patient or their legal representative; 2. Compliance with the study protocol and follow-up procedures; 3. Patients aged >=18 and = 9.0 g/dL (may be maintained or achieved via blood transfusion); 7. Absolute neutrophil count >=1.5×10^9(/L; 8. Platelet count >=50×10^9/L; 9. Serum creatinine =60 mL/min; 10. For patients not receiving anticoagulant therapy, prothrombin time international normalized ratio (INR) <=1.5 and activated partial thromboplastin time (APTT) <=1.5 × ULN. Patients on full-dose or parenteral anticoagulation may be enrolled if the anticoagulant dose has been stable for at least two weeks prior to study entry and coagulation test results are within the therapeutic range required for local treatment; 11. Women of childbearing potential (aged 15–49) must have a negative urine pregnancy test within 7 days before initiating treatment.

Exclusion criteria

Exclusion criteria: 1. Diagnosis of malignant tumors at other sites within the past 5 years; or presence of brain, lung, bone metastases, or abdominal lymph node metastasis; 2. Severe cardiopulmonary, hepatic, or renal insufficiency; 3. Pregnant or lactating women; 4. Any condition that may compromise patient safety or study data integrity, including significant medical risk factors, medical disorders, or laboratory abnormalities; 5. HIV or syphilis infection; 6. Investigator’s judgment that the patient is unsuitable for participation in this trial; 7. Unwillingness or inability to comply with study procedures, or anticipated absence from observation for one or more treatment cycles during the study.

Design outcomes

Primary

MeasureTime frame
Intraoperative Blood Loss;Operative Time;Pancreatic Fistula Rate;

Secondary

MeasureTime frame
Postoperative Complication Rate;Length of Postoperative Hospital Stay;Reoperation Rate;90-Day Mortality Rate;

Countries

China

Contacts

Public ContactZhiming Zhao

Chinese People’s Liberation Army General Hospital

zhaozhiming153@126.com+86 10 6687 5532

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026