Lidocaine Infusion in Pancreatic Cancer

Description

This study elucidates the effects of the intravenous (IV) lidocaine infusion on the biology of pancreatic circulating tumor cells (CTCs) isolated from patients undergoing robotic pancreatectomy for all types of pancreatic cancer. A prospective randomized controlled double blinded trial design will be used for the proposed study.

Conditions

Pancreatic Cancer

Study Overview

Study Details

Study overview

This study elucidates the effects of the intravenous (IV) lidocaine infusion on the biology of pancreatic circulating tumor cells (CTCs) isolated from patients undergoing robotic pancreatectomy for all types of pancreatic cancer. A prospective randomized controlled double blinded trial design will be used for the proposed study.

Lidocaine Infusion in Pancreatic Cancer: Translational Studies in a Preclinical Model And Human Subjects

Lidocaine Infusion in Pancreatic Cancer

Condition
Pancreatic Cancer
Intervention / Treatment

-

Contacts and Locations

Chicago

University of Illnois at Chicago, Chicago, Illinois, United States, 60612

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Has histologically or cytologically confirmed adenocarcinoma of the pancreas that is considered resectable as well as other types of pancreatic cancer (malignant endocrine and exocrine tumors)
  • 2. Has measurable disease, defined as at least 1 tumor that fulfills the criteria
  • 3. Patients diagnosed with resectable cancer, but upon initial phase of surgical exploration found to have metastatic disease
  • 4. Has read, understood and signed the informed consent form (ICF) approved by the Independent Review Board/Independent Ethics Committee (IRB/IEC)
  • 5. Prior systemic treatments for metastatic disease are permitted, including targeted therapies, biologic response modifiers, chemotherapy, hormonal therapy, or investigational therapy.
  • 1. Has American Society of Anesthesiologists (ASA) physical status \> 3
  • 2. Has hypersensitivity or allergy to amide-linked local anesthetics
  • 3. Has a second or third degree heart block
  • 4. Has severe sinoatrial block
  • 5. Is currently being treated with any of the following class I antiarrhythmic drugs; quinidine, flecainide, disopyramide, or procainamide
  • 6. Has been treated with amiodarone in the past
  • 7. Has Adams-Stoke syndrome
  • 8. Has Wolff-Parkinson-White syndrome
  • 9. Has a history of blood clots, pulmonary embolism, or deep vein thrombosis unless controlled by anticoagulant treatment
  • 10. Has a known history of human immunodeficiency virus (HIV) positivity or untreated and uncontrolled hepatitis B or C

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Illinois at Chicago,

Gina E. Votta-Velis, MD PhD, PRINCIPAL_INVESTIGATOR, Associate Professor

Study Record Dates

2025-01-01