Epidural block: Epidural block (with 0.375% ropivacaine) is performed during surgery. Patient-controlled epidural analgesia (with a mixture of 0.12% ropivacaine and 0.5 microgram/ml sufentanyl) is provided after surgery.
Dexamethasone: Dexamethasone (10 mg) is administered intravenously before anesthesia induction.
Study summary
Pancreatic cancer remains a devastating disease with an average 5-year survival rate of about 3-5%. Previous retrospective studies showed that perioperative epidural block and/or dexamethasone are associated with improved outcome after cancer surgery. This randomized trial aims to investigate the effect of perioperative epidural block and/or dexamethasone on long-term survival in patients following pancreatic cancer surgery.
Eligibility
Sex
ALL
Min age
45 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria:
1. Age ≥45 and \<90 years;
2. Clinically diagnosed as resectable or possibly resectable pancreatic cancer and scheduled to undergo radical surgery;
3. Agreed to receive epidural block and postoperative patient-controlled analgesia;
4. Agreed to participate in the study and provided written informed consent.
Exclusion Criteria:
1. Clinical evidence of unresectable pancreatic cancer or plan to undergo biopsy;
2. Previous surgery for pancreatic cancer, scheduled to undergo resurgery for recurrence or metastasis;
3. Complicated with primary malignant tumor in other organ(s), either previously or at present;
4. Complicated with autoimmune diseases, receiving either glucocorticoids or other immunosuppressants before surgery;
5. Unable to complete preoperative evaluation due to severe dementia, language barrier, coma, or end-stage diseases;
6. 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;
7. 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;
8. Other conditions that are considered unsuitable for study participation;
9. Refused to participate in the study.
Primary outcome measure(s)
2-year overall survival — Up to 2 years after surgery. 2-year overall survival
Trial sites (1)
Facility
City
Region
Status
Peking University First Hospital
Beijing
Beijing Municipality
More Peking University First Hospital trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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