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Study identifier: NCT06118710 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of the Omission of Dexamethasone in Premedication Regimens During Paclitaxel Treatment

Condition: Cancer  ·  Sponsor: Erasmus Medical Center

PhasePhase 4
Planned participants500
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This prospective multicenter randomized non-inferiority trial aims to assess whether omitting dexamethasone from the premedication regimen during paclitaxel-based chemotherapy is non-inferior to the standard of care regimen that includes dexamethasone, based on the incidence of clinically relevant hypersensitivity reactions (HSRs) of grade ≥3 as per CTCAE v5.0. With a study population of 500 adult patients with solid tumors, the trial will also investigate secondary endpoints including the severity and incidence of HSRs of any grade, the number of paclitaxel administrations until the first HSR, the impact on patients' quality of life, adverse events related to dexamethasone, and the cost-effectiveness of the two premedication regimens from healthcare and societal perspectives.

This description comes directly from the study's public registry record.

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Locations (1)

Erasmus MCRotterdam, South Holland, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT06118710