Clinical Trials Directory

Trials / Completed

CompletedNCT00271973

OXY-2: The Pharmacogenetics of Oxycodone Analgesia in Human Experimental Pain Models

The Pharmacogenetics of Oxycodone Analgesia in Human Experimental Pain Models

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
32 (planned)
Sponsor
Odense University Hospital · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers
Accepted

Summary

Thirty-two healthy volunteers will be submitted to experimental pain and on the 2 study days receive Oxycodone 20 mg po vs. placebo. Half of the volunteers will be poor metabolizers according to CYP2D6 genotype and half will be extensive metabolizers (EM) and have an enzyme with normal function. The study hypothesis is that PM will experience less pain relief than EM.

Detailed description

Oxycodone is a semi-synthetic opioid with an analgesic effect in the postoperative pain management comparable to morphine. Oxycodone is N-demethylated by CYP2D6 to its active metabolite oxymorphone, a potent μ-receptor agonist. A genetic polymorphism divides a Caucasian population into two groups: 8% with an enzyme lacking activity, poor metabolizers (PM) and the rest with normal CYP2D6 activity, extensive metabolizers (EM). Many different, single nucleotide polymorphisms (SNPs) are responsible for interindividual differences in the effect of opioids. Among these are the A118G SNP in the μ-receptor gene OPRM1 and the C3435T and G2677T/A SNPs in the MDR-1 gene of P-glycoprotein. P-glycoprotein is responsible for the absorption, excretion and transport of many drugs including opioids over the blood-brain barrier. Electrical stimulation and cold pressor test are among the most well defined and evaluated human experimental pain models. The 32 volunteers will be submitted to the tests before and 1, 2, 3 and 4 hours after medicine intake. To determine the plasma levels of Oxycodone and its metabolites blood will be drawn after each pain test. Also the CYP2D6 genotype and the above mentioned SNPs will be determined from the blood samples.

Conditions

Interventions

TypeNameDescription
DRUGOxycodone

Timeline

Start date
2006-02-01
Completion
2007-01-01
First posted
2006-01-04
Last updated
2007-01-30

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00271973. Inclusion in this directory is not an endorsement.