Continuous Lidocaine Infusion for Management of Perioperative Burn Pain

Completed · Phase 4 · Has a placebo group

Conditions studied: Thermal Burns

In brief

Thermal injury results in one of the most intense and prolonged forms of pain the body can experience. Opioid narcotics are the most powerful drugs for acute and chronic pain, and their use in the perioperative period has been the mainstay of treatment; although medication requirements in burn patients are often underestimated. More medication may not be the answer, as relatively large doses of short acting opioids in the operative theater are associated with greater postoperative opioid consumption and higher pain scores. Furthermore, extensive use of opioids has resulted in the development of by hyperalgesia and allodynia. Lidocaine is an amide local anesthetic that has analgesic, anti-hyperalgesic, antiarrhythmic, and anti-inflammatory properties. Over the past 25 years, systemic lidocaine has been used for perioperative pain management in a variety of surgical procedures. The design of this study will examine if lidocaine will reduce the pain scores and narcotic utilization in patients undergoing surgical procedures for burn injuries. The intervention group will receive a bolus dose of lidocaine followed by a continuous infusion over 24 hours. The control group will get an equal volume of saline. The investigators will compare pain scores, opioid use, and narcotic equivalents based on body weight and burn surface area (BSA) grafted.

Key facts

Study ID

NCT02059902

Run by

HealthPartners Institute

People needed

36

Starts

2012-09-01

Expected to finish

2015-02-01

Last updated by the study team

2018-07-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Burn patient ≥ 18 years of age
• Burn patient scheduled to go to OR for excision and/or grafting procedure

You may not qualify if…

• Burn patient < 18 years of age
• Intubated patient on sedation drip
• Prolonged hypotension defined as Systolic Blood Pressure (SBP) < 90 mm/Hg for greater than 30 minutes in the pre-op area
• Severe underlying cardiovascular disease (documented ejection fraction < 40%)
• Documented conduction block, bradycardia or active congestive heart failure
• Documented active gastritis or ulcers
• Previous steroid medication history if documented adrenal insufficiency
• Patient with documented liver disease
• Patient with epilepsy or known seizure disorder
• Pregnant Women

Where it is running

• Regions Hospital — Saint Paul, Minnesota, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.