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Study of Ketamine Administered Intravenously and by Sublingual Wafer

Pain Clinical Trial

Official title:
An Open Label, Two Way Crossover Study to Evaluate the Bioavailability and Clinical Tolerability of a Novel Sublingual Wafer Formulation of Ketamine in Healthy Male Volunteers

Clinical Trial Summary

To determine the rate and extent of of absorption of racemic ketamine from sublingual wafer

Clinical Trial Description

1. To determine the apparent rate of disintegration of the sublingual wafer

2. To determine the overall clinical tolerability of ketamine when administered as a single dose via the sublingual route. Tolerability will be assessed using a range of objective and subjective parameters as assessed using modified Likert and Bond and Lader scales. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01377831
Study type Observational
Source iX Biopharma Ltd.
Contact
Status Completed
Phase N/A
Start date June 2011
Completion date June 2011
View Details
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