CClinicalTrials.gg
Status unknownNCT00773760Updated Aug 6, 2009

MOR and COMT SNP Polymorphism and Pain

An observational study in Pain Relief, sponsored by East Tallinn Central Hospital. Status unknown at 1 site in Estonia. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2009-08-06.

Sponsored by East Tallinn Central Hospital · Observational

The sponsor has not verified this record recently (last verified Aug 2009), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Patients with certain polymorphism in the MOR and COMT genes will display differences in their response to analgesics.

Read the detailed description

After tissue injury, there is great interindividual variability among patients in the amount of pain experienced (pain intensity and duration of pain) and in the degree of pain relief from analgesics. In experimental settings, Single Nucleotide Polymorphisms (SNP) at the MOR and COMT genes have been found to alter the response to opioids in in vitro models and in human.We will collect clinical data on one hundred patients undergoing surgery. We will obtain DNA extracted via PCR techniques from the patients' blood and we will identify SNPs at the mu opioid receptor and catechol-O-methyltransferase genes. We will analyze the data to search for correlation between clinical patterns of postoperative pain and opioid effects and SNPs.

02

Conditions studied

  • Pain Relief

Keywords

  • opioids
  • COMT
  • SNP
  • analgesia
  • postoperative pain
03

In context

Lead sponsor

East Tallinn Central Hospital is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

patients with prostate cancer

Inclusion criteria

  • 18 years of age and older
  • Give informed consent to participate in this study

Exclusion criteria

Exclusion Criteria:

  • Neurologic or psychiatric disease sufficient, in the clinical judgment of the investigator, to compromise informed consent or data collection
  • ASA classification score 3 or above
  • Patients with past or present history of substance abuse.
  • Patients with a history of chronic pain requiring daily analgesic use for more then one month.
  • Patients with a current diagnosis of anxiety or depression requiring medical treatment
  • Patients allergic to morphine
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Biospecimen retention
Samples with dna

Groups and cohorts

  • dosing

    Other: SNP genotyping

Interventions

  • OtherSNP genotyping

    Coded blood specimens will be transported to the Department of Gene Technology TTÜ and genotyping analysis will be performed. Lymphocytes will be isolated from blood specimens using Ficol-Paq gradients, and genomic DNA isolated using a salting-out procedure. Variants of the MOR gene and other genes of interests will be performed by DNA sequence analysis of PCR-amplified DNA, using primers located in flanking intron sequence. All methods proposed are currently in operation in the respective facilities.

06

What researchers measure

Primary outcomes

  1. Postoperative assessments include PCA use (e.g., number of patient demands, total morphine administered) in each 24-h interval during the 48-h study period - primary endpoint.

    Time frame: 48 hours

Secondary outcomes

  1. No secondary outcome endpoint

    Time frame: no time frame

07

Study locations

1 of 1 sites recruiting
  • Yuri Kolesnikov MD PhD
    Tallinn, 11312, Estonia
    • Peeter Ross, MD · Contact · peeter.ross@itk.ee · 372 6973002
    • Yuri Kolesnikov · Contact · yuri.kolesnikov@itk.ee · 372 6973002
    • Boris Gabovits, MD · Sub investigator
    • Yuri Kolesnikov, MD PhD · Principal investigator
    Recruiting
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 6, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00773760
Lead sponsor
East Tallinn Central Hospital
First posted
Oct 16, 2008
Start date
Oct 2008
Primary completion
Oct 2009 (estimated)
Completion
Dec 2009 (estimated)
Last update
Aug 6, 2009

Study contacts

Yuri Kolesnikov, MD PhD
study director · ETCH

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2009. You cannot join it, but the record below documents what was studied.

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