Active — Not RecruitingPhase 2

Juice Plus+ and Juice Plus+ Complete in Ovarian Cancer

United States75 participantsStarted 2003-02-18

Plain-language summary

The goal of this clinical research study is to see if ovarian cancer patients who add Juice PLus+ and Juice Plus+ Complete to their diets have better outcomes when compared to ovarian cancer patients who receive only dietary counseling alone.

Who can participate

Age range

21 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Body Mass Index (BMI) \> 19.5
. Epithelial ovarian cancer of (any tumor type). Stages 2 and up.
. In first clinical remission. (CA125 \< 35)
. \> 21 years of age.
. CT scan of abdomen/pelvis without evidence of ovarian cancer.
. Ambulatory/mobile and able to eat/not on parenteral nutrition.
. Life expectancy of at least 6 months.
. Informed consent signed indicating patient's knowledge of the investigational nature of the study.

Exclusion criteria

. Evidence of bowel obstruction.
. Pregnant or lactating.
. Diagnosed with a co-morbidity requiring a restricted diet or medication for which a high fiber diet may be contraindicated.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change in serum lipid peroxide levels resulting from nutritional supplements or dietary counseling

Timeframe: Baseline to 6 months

Change in levels of serum carotenoid resulting from nutritional supplements or dietary counseling

Timeframe: Baseline to 6 months

Trial details

NCT IDNCT01439659

SponsorM.D. Anderson Cancer Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-03-01

View on ClinicalTrials.gov More Ovarian Cancer trials