Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Salt Lake City, Utah


Purpose:

The primary aim of this study is to investigate if AZD1940 can relieve the pain induced by the surgical removal of one lower wisdom-tooth. This will be done by comparing the effect of AZD1940 to placebo ("inactive substance") on pain. A number of patients will instead receive the common painkiller naproxen for comparison purposes. Rescue medication, acetaminophen, will be allowed if a need for additional painkillers would arise. A number of patients will receive Naproxen as control.


Criteria:

Inclusion Criteria: - Patients scheduled for surgical removal of one partial or complete impacted mandibular third molar. - Provision of signed informed consent. - Healthy males or non-fertile females. Exclusion Criteria: - History of somatic disease/condition, which may interfere with the objectives of the study, as judged by the investigator. - History of previous or ongoing psychiatric disease/condition including psychosis, affective disorder, anxiety disorder, borderline state and personality disorder according to the criteria in the Diagnostic and Statistical Manual of Mental Disorder, 4th edition.


NCT ID:

NCT00659490


Primary Contact:

Principal Investigator
Lynn Webster, MD
Lifetree Clinical Research3838 South, 700 East, Suite 202Salt Lake City, Utah 84106, USA


Backup Contact:

N/A


Location Contact:

Salt Lake City, Utah
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 23, 2018

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.