Intravenous Lidocaine Infusion in the Management of Post-operative Pain in Colorectal Patients

Withdrawn before enrolling · Phase 1/Phase 2

Conditions studied: Colorectal Disorders

In brief

The purpose of this study is to determine if an intravenous lidocaine infusion (compared to placebo) intraoperatively will decrease time to return of bowel function postoperatively, decrease postoperative pain, diminish postoperative opioid requirement, minimize inflammatory markers and shorten time to discharge after colorectal surgery.

Key facts

Study ID

NCT01836614

Run by

Children's Hospital Medical Center, Cincinnati

People needed

0

Starts

2015-01-01

Expected to finish

2018-04-01

Last updated by the study team

2016-03-08

Who can join

Age: 1 and older, up to 15. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• male or female children 1-15 years of age
• ASA physical status 1-3
• scheduled for colorectal surgery with abdominal incision
• scheduled for complex urology surgical case

You may not qualify if…

• ASA physical status > 3
• postoperative intubation planned ahead of surgery
• history of chronic use of opioid
• history of hepatic,renal, or cardiac failure
• history of organ transplant
• BMI > 30
• history of cardiac arrhythmia
• history of long QT syndrome
• history of allergic reaction to lidocaine or similar agents
• history of seizure disorder
• patient without Peripherally Inserted Central Catheter or other central access with contraindication to inhalation induction
• family history or know patient susceptibility to malignant hyperthermia

Where it is running

• Cincinnati Children's Hospital Medical Center — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

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