IV Lacosamide: The Safety of Intravenous Lacosamide
Completed · Phase 3
Conditions studied: Epilepsy
In brief
The purpose of this study is to evaluate the safety of IV Lacosamide in children ages 4-35.
Key facts
- Study ID
- NCT01981447
- Run by
- Le Bonheur Children's Hospital
- People needed
- 40
- Starts
- 2010-04-01
- Expected to finish
- 2012-08-01
- Last updated by the study team
- 2020-09-22
Who can join
Age: 4 and older, up to 35. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patient or LAR must sign informed consent
- Diagnosis of partial onset currently uncontrolled
- Patient must have received anti-epileptic drug therapy prior to initiation
- Patient must have a medical condition in which parental administration is desireable
- Male or female
- Ages 4-35
You may not qualify if…
- Patient has participated in a study involving IV Lacosamide
- Patient has had an episode of status epilepticus in the last 3 months
- Drug history to lacosamide pregnant or lactating
- If of child bearing age, must have pregnancy test
- Patient has participated in an experimental drug study in last 30 days
- Patients with significant active hepatic or renal disease.
- Patients with known cardiac disease.
Where it is running
- Lebonheur Children's Hospital — Memphis, Tennessee, United States
Full record on ClinicalTrials.gov
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