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

Mouth and Tooth DiseasesTooth, Impacted

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

This trial is not recruiting

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

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source