Ovarian Cancer Clinical Trial
Study of Nutritional Supplement Shakes in People About to Receive Their Debulking Surgery for Ovarian Cancer
Summary
The purpose of this study is to find out if it is possible to establish a nutritional support program for people who are scheduled to receive primary debulking surgery.
Design: This will be a prospective observational study to assess the feasibility of implementing a preoperative nutrition supplementation program.
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18
Scheduled to undergo primary surgical debulking of ovarian, fallopian tube and primary peritoneal cancer
Have a sufficient preoperative window during which the intervention can occur, with the last day of supplementation at least one and no more than two days prior to surgery; scheduling of the procedure should not be delayed due to participation in this investigation
Exclusion Criteria:
Have received neoadjuvant chemotherapy
Debulking surgery scheduled less than 8 days from initial visit
Are scheduled for a minimally invasive procedure
Unable to tolerate oral intake or have gastrointestinal issues that would prevent or prohibit oral supplement consumption
Have diabetes mellitus
Have allergies to the Ensure Surgery Immunonutrition Shake supplement
Have galactosemia
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There are 8 Locations for this study
Miami Florida, 33143, United States
Basking Ridge New Jersey, 07920, United States
Middletown New Jersey, 07748, United States
Montvale New Jersey, 07645, United States
Commack New York, 11725, United States
Harrison New York, 10604, United States
New York New York, 10065, United States
Uniondale New York, 11553, United States
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