Clinical Trials Directory

Trials / Completed

CompletedNCT00232492

Ketamine on Acute Pain in Females and Males

Effect of Racemic Ketamine on Pain in Females and Males After Surgical Removal of Third Molars

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
128 (actual)
Sponsor
Ullevaal University Hospital · Academic / Other
Sex
All
Age
20 Years – 30 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

Ketamine is assumed to be a NMDA receptor antagonist which provides analgesia from acute postoperative pain(and other types of pain) subanesthetic doses. Gender differences in ketamine analgesia are not known. This placebo-controlled,randomised, parallel group study investigates the analgesic dose-response effect of ketamine in subanesthetic doses in female and male patients following surgical removal of third molars. Comparisons: Placebo and ketamine in females and males.

Conditions

Interventions

TypeNameDescription
DRUGPlacebo malesIntravenous saline bolus (Placebo-control) males
DRUGKetamine 0,1 mg/kg males0,1 mg/kg ketamine iv bolus males
DRUGKetamine 0,3 mg/kg males0,3 mg/kg ketamine iv bolus males
DRUGKetamine 0,5 mg/kg males0,5 mg/kg ketamine iv bolus males
DRUGPlacebo femalesIntravenous saline bolus (Placebo-control) females
DRUGKetamine 0,1 mg/kg females0,1 mg/kg iv bolus ketamine females
DRUGKetamine 0,3 mg/kg females0,3 mg/kg iv bolus ketamine females
DRUGKetamine 0,5 mg/kg females0,5 mg/kg iv bolus ketamine females

Timeline

Start date
2005-01-01
Primary completion
2006-11-01
Completion
2006-11-01
First posted
2005-10-04
Last updated
2011-07-06

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT00232492. Inclusion in this directory is not an endorsement.