WHO ICTRP trial

A phase II randomised study to evaluate the efficacy of aprepitant plus…

JPRN-UMIN000019122 · Japan Primary Registries Network (JPRN) · Not Recruiting

Key facts

Trial ID JPRN-UMIN000019122
Public title A phase II randomised study to evaluate the efficacy of aprepitant plus palonosetron for preventing delayed-phase CINV associated with TC therapy in gynaecological cancer
Scientific title A phase II randomised study to evaluate the efficacy of aprepitant plus palonosetron for preventing delayed-phase CINV associated with TC therapy in gynaecological cancer - A phase II randomised study to evaluate the efficacy of aprepitant plus palonosetron for preventing delayed-phase CINV…
Primary sponsor Juntendo Nerima Hospital
Registry Japan Primary Registries Network (JPRN)
Recruitment status Not Recruiting
Study type Interventional
Phase Not selected
Countries Japan
Conditions gynaecological cancer
Interventions control group (standard antiemetic therapy:0.75 mg palonosetron administered intravenously on day 1 and 6 mg dexamethasone administered intravenously on day 1 and 4 mg dexamethasone administered orally on days 2 and 3). aprepitant group…
Registration date Sep 26, 2015
Target size 76
Registry page center6.umin.ac.jp

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