Breast Cancer Clinical Trial
Official title:
Feasibility of a Randomized Controlled Clinical Trial Comparing the Use of Cetirizine to Replace Diphenhydramine in the Prevention of Reactions Related to Paclitaxel
Explore the randomized, controlled, double-blind design targeted for the final clinical trial to assess the acceptability of interventions and clinical outcome measures and to provide data making it possible to estimate the parameters necessary for the preparation, modification or even abandonment of the final study.
Paclitaxel is known to cause 30 to 40% of infusion-related reactions when no premedication is
administered. It is agreed that all patients should receive premedication with dexamethasone,
an H1 antagonist, such as diphenhydramine, and an H2 antagonist before the administration of
paclitaxel. There are several cases where undesirable effects (eg. drowsiness, dry mouth,
motor impatience) have been reported following the administration of this conventional
premedication. Diphenhydramine is often accused because of its pharmacological properties.
A definitive, randomized, double-blind, non-inferiority study can assess whether cetirizine,
a non-sedating H1 antagonist, can be used as an effective and safe alternative to
diphenhydramine in the prevention of paclitaxel infusion-related reactions.
In the current proposed feasibility study, patients will be followed for the first two doses
of paclitaxel. The goal is to explore the randomized, controlled, double-blind design
targeted for the final clinical trial to assess the acceptability of interventions and
clinical outcome measures and to provide data making it possible to estimate the parameters
necessary for the preparation, modification or even abandonment of the final study.
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