Cancer-related pain Strong-acting opioids Pharmacogenetic(s) Pharmacokinetics Opioid rotation Pain control Side effects Kanker gerelateerde pijn sterk werkende opioiden Farmacogenetica Farmacokinetiek Opioid rotatie Pijncontrole Bijwerkingen
Conditions
Interventions
Treatment is given according to physician's choice
Blood samples drawn for pharmacogenetic analysis in all patients
Blood samples drawn for pharmacokinetic analysis in patients who consent only
Sponsors
Erasmus MC Cancer Institute, Rotterdam, the Netherlands
Eligibility
Inclusion criteria
Inclusion criteria: Hospitalized patients treated with strong-acting opioids for moderate to severe cancer related nociceptive pain. Starting treatment with strong-acting opioids or needing adjustment of current treatment
Exclusion criteria
Exclusion criteria: Estimated duration of hospitalisation < 72 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Are variations in pharmacogenetics and/or pharmacokinetics related to insufficient pain control and/or the occurrence of intolerable side effects? - To study the role of demographic and clinical factors on outcome of treatment - To study how the factors mentioned above affect the outcome of opioid rotation | — |
Contacts
Public ContactA, Oosten
P.O. Box 5201, 3008 AE Rotterdam, The Netherlands
Outcome results
None listed