Overview

Effect of Perioperative Intravenous Lidocaine Infusion in Robotic-Assisted Urologic Surgery

Status:
Recruiting
Trial end date:
2022-03-01
Target enrollment:
0
Participant gender:
All
Summary
Controlling pain is fundamental during and after surgical procedures. This study examines pain associated with robotic assisted surgery on prostate cancer or a kidney mass. In recent years, the risk of opioids in the postoperative period has gained interest due to the growing epidemic of addiction, dependence, and overdose. In this study, the investigators expect a continuous infusion of intravenous lidocaine during the perioperative period to result in less pain and less opioid use.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Missouri-Columbia
Treatments:
Lidocaine
Pharmaceutical Solutions
Criteria
Inclusion Criteria:

- Undergoing robotic assisted prostatectomy or robotic assisted partial nephrectomy at
University of Missouri Hospital for prostate cancer or kidney mass

- Age ≥ 18 years

- ASA I-III

Exclusion Criteria:

- Inability to obtain written informed consent

- Allergy to lidocaine or other amide local anesthetics

- Atrioventricular conduction blocks

- CV instability and concomitant use of alpha agonists or beta blockers

- Recent myocardial infarction (≤ 6 months ago)

- Cardiac arrhythmia disorders

- Stokes-Adams syndrome

- Wolff-Parkinson-White syndrome

- Seizure disorders

- Liver failure or hepatic dysfunction

- Significant renal disease with a serum creatinine ≥ 2 mg/dl

- A family history of malignant hyperthermia

- Current use of opioids or documented history of opioid abuse

- Typically, have less than 3 bowel movement per week

- Combined surgical cases that include robotic prostatectomy or robotic partial
nephrectomy