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Effect of continuous intravenous infusion of lidocaine on postoperative recovery and long-term outcomes of patients with pancreatic cancer: A prospective, randomized controlled trial

Effect of continuous intravenous infusion of lidocaine on postoperative recovery and long-term outcomes of patients with pancreatic cancer: A prospective, randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035469
Enrollment
Unknown
Registered
2020-08-12
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Pancreatic cancer

Interventions

Lidocaine Group :Intravenous infusion of lidocaine
Control Group:Intravenous infusion of saline

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. aged 18 to 70 years old; 2. resectable pancreatic head cancer diagnosed; 3. ECOG stage 0-2; 4. More than 2 weeks from the end of the last chemotherapy; 5. Total bilirubin level =10 g/dL, platelet count greater than 100x10^9/L; 7. serum creatinine <2.5 ULN; 8. have carefully read and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Diagnosed as unresectable pancreatic cancer; 2. ASA grade greater than grade 3; 3. Patients with a history of local anesthetic drug allergy; 4. History of severe sinus block and other arrhythmia; 5. Currently receiving any of the following class I antiarrhythmics Drug treatment: Quinidine, Flecainide, Disopyramide or Procainamide; 6. Previous use of amiodarone hydrochloride treatment; 7, Autoimmune disease patients or untreated and untreated type B or C Hepatitis; 8. Have a history of pulmonary embolism or deep vein thrombosis.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Disease-free survival;Postoperative complication rate;Length of Stay;

Countries

China

Contacts

Public ContactChen Wankun

Zhongshan Hospital, Fudan University

chenwank@163.com+86 18017317651

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026