Skip to content

Perioperative Intravenous Lidocaine Infusion Reduces the Risk of Postoperative Recurrence and Metastasis of Pancreatic Cancer: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial

Perioperative Intravenous Lidocaine Infusion Reduces the Risk of Postoperative Recurrence and Metastasis of Pancreatic Cancer: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127030
Enrollment
Unknown
Registered
2026-06-23
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Pancreatic cancer

Interventions

Trial group:Lidocaine intravenous infusion: Intravenous injection of 1.5 mg/kg based on ideal body weight (IBW) during anesthesia induction, completed within 10 minutes, followed by continuous infusio
Placebo group:Placebo (0.9% saline): Intravenous injection of saline 1.5 ml/kg during anesthesia induction (mimicking volume and rate of lidocaine bolus), followed by continuous infusion of saline at

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 80; 2.American Society of Anesthesiologists (ASA) classification of grades I-III; 3.Patients diagnosed with pancreatic cancer (or other periampullary cancers) through imaging and/or pathology, who plan to undergo definitive radical pancreatectomy (such as pancreaticoduodenectomy, distal pancreatectomy, etc.) within a limited timeframe; 4.Agree to use patient-controlled analgesia (PCA) device for postoperative pain management; 5.Sign the informed consent form and voluntarily comply with the research protocol and follow-up requirements;

Exclusion criteria

Exclusion criteria: 1.weight under 40kg; 2.Combined with other active malignant tumors; 3.Preoperative assessment indicated palliative surgery or exploratory surgery without the possibility of radical resection; 4.Autoimmune disease; 5.Severe hepatic insufficiency (aspartate aminotransferase or alanine aminotransferase or bilirubin > 2.5 times the upper limit of normal); 6.Severe renal insufficiency (serum creatinine =186µmol/L or creatinine clearance rate 3 months) regular use of opioids;

Design outcomes

Primary

MeasureTime frame
Disease-Free Survival(DFS);

Secondary

MeasureTime frame
The incidence rate of major complications within 30 days after surgery;Total consumption of opioids;Postoperative hospitalization duration;Postoperative pain score, postoperative sleep score;Recurrence/metastasis rate;Incidence of postoperative cognitive dysfunction;Dynamic changes of perioperative inflammatory/immune biomarkers;Postoperative ICU admission rate;First exhaust time;Overall Survival(OS);Incidence of postoperative delirium;

Countries

China

Contacts

Public ContactZhang Liyun

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

zlzhangliyun@126.com+86 21 64370045

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026