Phase
Condition
Pancreatic Disorders
Treatment
Main pancreatic duct and biliary duct external drainage
Main pancreatic duct and biliary duct internal drainage
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Signed informed content obtained prior to treatment
Age ≥ 18 years and ≤ 80 years
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. Lifeexpectancy ≥12 weeks and ASA score ≤2.
Based on clinical symptoms, imaging examinations, tumor markers, and other auxiliaryexaminations, the clinical diagnosis includes but is not limited to tumors of thepancreatic head, ampulla of Vater, duodenum, and distal common bile duct, requiringpancreaticoduodenectomy.
No serious dysfunction in blood system, heart, lung function, or autoimmune system (refer to the respective diagnostic criteria)
White blood cell (WBC) ≥ 3 × 109/L; Absolute neutrophil count (ANC) ≥ 1.5 × 109/L;Platelets (PLT) ≥ 100 × 109/L; Hemoglobin (Hgb) ≥ 90 g/L
Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]/alanine aminotransferase (ALT) (serum glutamic pyruvate transaminase [SGPT]) ≤ 2.5 ×institutional upper limit of normal (ULN); Total bilirubin (TBIL) ≤ ULN; Creatinine (CRE) ≤ 1.5 × ULN
Prothrombin time (PT) and international normalized ratio (INR) ≤ 1.5 × ULN
Able to comply with research visit plans and other protocol requirements.
With intermediate or high risk of postoperative pancreatic fistula (POPF) accordingto alternative fistula risk scoring system (A-FRS)
Exclusion
Exclusion Criteria:
Cancer in late stage including distant organ metastasis (liver, lung, peritoneum),metastasis to the hilar bile duct and hepatic duct, extensive metastasis to thehepatic portal lymph nodes, tumor invasion of the superior mesenteric artery, celiactrunk, inferior vena cava, or abdominal aorta.
Heart Failure: Congestive heart failure with New York Heart Association (NYHA) heartfunction classification of 3 or 4.
Uncontrolled Hypertension:
Renal Failure: Renal failure or insufficiency requiring hemodialysis or peritonealdialysis.
Active Infection: Serious active clinical infection (> Grade 2, NCI-CTCAE version 4.0).
Pregnancy or Lactation: Pregnant or lactating women.
Major Surgery: Patients who have undergone major surgery within 4 weeks of startingthe trial or have not recovered from the side effects of such surgery.
Other Malignancies: Combined with other malignant tumors (patients who have beencured 3 years ago can be included).
Upper Gastrointestinal Bleeding: Excluding patients with upper gastrointestinalbleeding within 4 weeks before surgery or with a clear tendency of gastrointestinalbleeding that cannot be corrected by active medical treatment.
Poor Compliance: Poor compliance, unable or unwilling to sign informed consent.
Study Design
Study Description
Connect with a study center
Zhongshan Hospital
Shanghai, Shanghai 200000
ChinaActive - Recruiting
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