Lamotrigine in Reducing Psychologic Side-Effect of Perioperative Ketamine

Completed · Phase 3 · Has a placebo group

Conditions studied: Reducing Psychological Side Effects of Ketamine

In brief

Patient will receive lamotrigine vs. placebo with small sips of water. Lamotrigine reaches peak level 1-4 hours after oral administration.

Key facts

Study ID

NCT03831854

Run by

The Cleveland Clinic

People needed

46

Starts

2019-01-24

Expected to finish

2020-12-31

Last updated by the study team

2021-06-09

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 -65 Years of age
• Planned overnight hospital stay

You may not qualify if…

• Pregnant and planning to become pregnant
• No known History of seizure
• No known History of Schizophrenia
• No known History of unstable angina
• Patients taking Antiepileptic medications
• Known history of Lamotrigine intake in past.
• Any history of allergic reaction to lamotrigine in the past.

Where it is running

• Cleveland Clinic — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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