Clinical trial
A Randomized,Double Blind, Parallel Group, Placebo Controlled Dose Ranging Study to Assess the Analgesic Efficacy, Tolerability, Safety and Pharmacokinetic/Pharmacodynamic Properties of a Sublingual Wafer Formulation of Ketamine Following Third Molar Extraction
NCT02199678 is registered in ClinicalTrials.gov with Lotus Clinical Research, LLC as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized,Double Blind, Parallel Group, Placebo Controlled Dose Ranging Study to Assess the Analgesic Efficacy, Tolerability, Safety and Pharmacokinetic/Pharmacodynamic Properties of a Sublingual Wafer Formulation of Ketamine Following Third Molar Extraction
- Lead sponsor
- Lotus Clinical Research, LLC
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- July 31, 2014
- Completion date
- November 30, 2014
- Enrollment
- 120 (actual)
- Sites
- 2
Conditions
As the registry lists them; a condition with its own page is linked.