Condition: Cancer Pain · Sponsor: Erasmus Medical Center
The primary objective is to evaluate the effect of loading boluses when dose incresaing treatment with SC fentanyl in patients with cancer. The primary endpoint of this study is to prove the non-inferiority of fentanyl plasma concentrations 12 hours after dose augmentation compared to 48 hours after dose augmentation within each patient. Patients will be treated with additional loading boluses and plasma-PK samples will be obtained.
This description comes directly from the study's public registry record.
Bram C Agema · +31107040704 · b.agema@erasmusmc.nl
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| Erasmus Medical Center | Rotterdam, South Holland, Netherlands | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06498037