Ketamine molecule:

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Ketamine Clinical Trials


A Randomized, Double-blind, Placebo-controlled, Cross-over Study to Assess the Safety, Tolerability and Efficacy of Oral Ketamine for Patients With Rett Syndrome


To see complete record on clinicaltrials.gov, please visit this link

Id: NCT03633058

Organisation Name: Rett Syndrome Research Trust

Overal Status: Recruiting

Start Date: March 12, 2019

Last Update: October 5, 2020

Lead Sponsor: Rett Syndrome Research Trust

Brief Summary: This 4 cohort, sequential, ascending dose study will assess the safety, tolerability and efficacy of oral ketamine dosed in a single 5-day BID regimen in addition to placebo, in a 4-week cross-over design in patients with Rett Syndrome. Approximately 12 patients per cohort and up to approximately 48 patients in total are anticipated to participate for approximately 8-10 weeks at approximately 7 US study centers.

Conditions:
  • Rett Syndrome


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