Perioperative Epidural Block and Dexamethasone in Pancreatic Cancer Surgery
Pancreatic Cancer, Surgery, Epidural Block
About this trial
This is an interventional supportive care trial for Pancreatic Cancer focused on measuring Pancreatic cancer, Radical resection, Epidural block, Dexamethasone, Overall survival
Eligibility Criteria
Inclusion Criteria:
- Age ≥45 and <90 years;
- Clinically diagnosed as resectable or possibly resectable pancreatic cancer and scheduled to undergo radical surgery;
- Agreed to receive epidural block and postoperative patient-controlled analgesia;
- Agreed to participate in the study and provided written informed consent.
Exclusion Criteria:
- Clinical evidence of unresectable pancreatic cancer or plan to undergo biopsy;
- Previous surgery for pancreatic cancer, scheduled to undergo resurgery for recurrence or metastasis;
- Complicated with primary malignant tumor in other organ(s), either previously or at present;
- Complicated with autoimmune diseases, receiving either glucocorticoids or other immunosuppressants before surgery;
- Unable to complete preoperative evaluation due to severe dementia, language barrier, coma, or end-stage diseases;
- Severe hepatic dysfunction (Child-Pugh C), severe renal insufficiency (serum creatinine >442 µmol/L or requirement of renal replacement therapy), or American Society of Anesthesiologists classification ≥V;
- Contradictions to epidural anesthesia, including spinal malformation, history of spinal surgery, coagulation disorder, suspected infection at the site of puncture, or severe low back pain;
- Other conditions that are considered unsuitable for study participation;
- Refused to participate in the study.
Sites / Locations
- Peking University First HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
No Intervention
Experimental
Experimental
Experimental
Control
Epidural block
Dexamethasone
Epidural block+Dexamethasone
Patients in this group receive general anesthesia, without epidural block and perioperative dexamethasone. Patient-controlled intravenous analgesia is provided after surgery.
Patients in this group receive combined epidural-general anesthesia (0.375% ropivacaine for epidural block), without perioperative dexamethasone. Patient-controlled epidural analgesia is provided after surgery.
Patients in this group receive dexamethasone (10 mg) before anesthesia induction and general anesthesia, without epidural block. Patient-controlled intravenous analgesia is provided after surgery.
Patients this group receive dexamethasone (10 mg) before anesthesia induction and combined epidural-general anesthesia (0.375% ropivacaine for epidural block). Patient-controlled epidural analgesia is provided after surgery.