Trial intelligence / Profile preview

Intravenous Lidocaine in Cystectomy

NCT02924480Completed

Sponsor
CAMC Health System
Start
Oct 2016
Primary completion
Jun 2020
Modality
Small Molecules
Countries
1
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Overview

Randomised, double-blind trial in postoperative pain and postoperative ileus (POI) comparing Lidocaine Study Group with Placebo Study Group (2 arms). Primary endpoints: Reduced pain post-operatively using verbal analog score at 108 hours and Time until Ileus resolution at 108 hours. Started Oct 2016; status: completed.

02

Drugs

Lidocaine Hydrochloride Injection, without epinephrine
03

Conditions

postoperative painpostoperative ileus (POI)

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