Nausea Clinical Trial
Official title:
Randomized Single-Blind Study of Nometex as an Adjunct to Standard Anti-emetics in Ovarian and Advanced Endometrial and Cervical Cancer Patients Who Receive Moderately to Highly Emetogenic Chemotherapy
The primary study hypotheses are that, without increasing doses of breakthrough medications
or device intolerance, the Nometex™ device worn for 5-days beginning with the day of
chemotherapy administration in women with ovarian or advanced endometrial or cervical cancer
will, as an adjunct to standard-of-care anti-emetics, reduce vomiting episodes, and reduce
the severity of nausea.
The secondary hypotheses are that the Nometex™ device reduces acute (Day 1) emetic episodes,
day 1 and days 2-5 severity of nausea, and delayed (days 2-5) emetic episodes without
increasing doses of breakthrough medications or device intolerance.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care
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