CompletedPhase 4ketamine
Ketamine on Acute Pain in Females and Males
Sponsored by Ullevaal University Hospital
NCT ID
NCT00232492
Target Enrollment
128 participants
Start Date
2005-01
Est. Completion
2006-11
About This Study
The purpose of the study is to determine whether equal subanesthetic doses of racemic ketamine is equally effective on females and males after surgical removal of third molars
Conditions Studied
Interventions
- •Placebo males
- •Ketamine 0,1 mg/kg males
- •Ketamine 0,3 mg/kg males
- •Ketamine 0,5 mg/kg males
- •Placebo females
- •Ketamine 0,1 mg/kg females
- •Ketamine 0,3 mg/kg females
- •Ketamine 0,5 mg/kg females
Eligibility
Age:20 Years - 30 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * Indication for removal of third molar * Between 20 and 30 years of age * ASA Class 1 Exclusion Criteria: * Psychiatric family (father/mother) or own anamnestic history * Hypersensitivity towards NSAIDS or other rescue analgesics * Verified or suspected pregnancy * Lactating females * Surgery lasting over 60 min
Study Locations (1)
Department of Oral and Maxillofacial Surgery, Ullevaal University Hospital
Oslo, Norway