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ABSTRACT: Objective
To evaluate the safety and efficacy of the granisetron transdermal delivery system (GTDS) combined with Dexamethasone for preventing chemotherapy-induced nausea and vomiting (CINV) in patients receiving Capecitabine plus Oxaliplatin (CapeOX) therapy.Design
Open-label, prospective, multi-center phase II trial.Setting
Three institutions.Participants
Fifty-four patients scheduled to receive CapeOX chemotherapy.Interventions
Participants received GTDS (3.1 mg applied to the upper arm 48 h before chemotherapy, replaced on day 5, and discarded on day 12) and Dexamethasone.Main outcome measures
The primary endpoint was the complete control rate of CINV. Secondary endpoints included the duration of delayed complete control, complete control
SUBMITTER: Wang C
PROVIDER: S-EPMC11264757 | biostudies-literature | 2024 Jul
REPOSITORIES: biostudies-literature