CompletedPhase 1ketamine

Pharmacokinetics and Pharmacodynamics of Nasally Applied Esketamine

Sponsored by University Hospital, Basel, Switzerland

NCT ID
NCT00847418
Start Date
2009-02
Est. Completion
2009-10

About This Study

The purpose of this study is the determination of blood concentration and the effectiveness of esketamine after nasal application.

Conditions Studied

Pain

Interventions

  • esketamine hydrochloride

Eligibility

Sex:MALE
Age:18 Years - 45 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* male
* age ≥18 years ≤ 45 years
* healthy
* non-smoking
* BMI 18-27

Exclusion Criteria:

* abuse of drugs
* known or supposed hypersensitivity and/or contraindication against ketamine or additives
* participation of another clinical study within the last 30 days
* chronic obstructed nose breathing or nasal polyps
* dug allergy
* blood donation within the last two months

Study Locations (1)

Clinical Research Center, University Hospital Basel
Basel, Canton of Basel-City, Switzerland

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source