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Carotenoid
Lycopene for Preventing Prostate Cancer
N/A
Waitlist Available
Led By Richard B. van Breemen, PhD
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
No existing gastrointestinal disease or cancer
No existing prostate disease
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Summary
This trial is testing if lycopene supplements, found in tomatoes, can prevent prostate cancer in healthy people. Lycopene might work by reducing damage from free radicals and affecting prostate health markers. Lycopene has been studied for its potential to reduce the risk of prostate cancer through its antioxidant properties and other mechanisms.
Who is the study for?
This trial is for healthy men who don't abuse alcohol or drugs, have no prostate disease or cancer, and aren't allergic to tomatoes. They must not be in the hospital, able to give blood and urine samples, and willing to answer health and diet questionnaires. Men already taking lycopene supplements or in another trial can't join.
What is being tested?
The study is testing if lycopene (a substance from tomatoes) can prevent prostate cancer when compared with a placebo (a harmless pill). Participants will be randomly assigned to receive either lycopene or the placebo without knowing which one they are getting.
What are the potential side effects?
Lycopene is generally considered safe but may cause digestive issues like bloating, indigestion, nausea, diarrhea; skin discoloration; and allergies in those sensitive to tomatoes.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I do not have any gastrointestinal diseases or cancer.
Select...
I do not have any prostate disease.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Side effects data
From 2014 Phase 4 trial • 28 Patients • NCT0258711769%
Flatulency
31%
Nausea
23%
Increased appetite
15%
Abdominal distension
15%
Diarrhea
8%
Headache
8%
Dizziness
100%
80%
60%
40%
20%
0%
Study treatment Arm
Lycopene Group
Prednisolone Group
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: Arm IIExperimental Treatment1 Intervention
Participants receive an oral tomato dietary supplement containing lycopene at a higher dose twice daily for 3 weeks.
Group II: Arm IExperimental Treatment1 Intervention
Participants receive an oral tomato dietary supplement containing lycopene twice daily for 3 weeks.
Group III: Arm IIIPlacebo Group1 Intervention
Participants receive oral placebo twice daily for 3 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
lycopene
2008
Completed Phase 4
~260
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for prostate cancer include antioxidants like lycopene, which may prevent cancer formation by neutralizing free radicals and reducing oxidative stress. Hormone therapy reduces androgen levels to slow cancer growth, while chemotherapy targets rapidly dividing cancer cells.
Understanding these mechanisms is crucial for selecting the most effective treatment based on the cancer's characteristics and the patient's health.
Lycopene for the prevention of prostate cancer.
Lycopene for the prevention of prostate cancer.
Find a Location
Who is running the clinical trial?
University of Illinois at ChicagoLead Sponsor
638 Previous Clinical Trials
1,568,979 Total Patients Enrolled
10 Trials studying Prostate Cancer
918 Patients Enrolled for Prostate Cancer
National Cancer Institute (NCI)NIH
13,906 Previous Clinical Trials
41,011,878 Total Patients Enrolled
515 Trials studying Prostate Cancer
332,738 Patients Enrolled for Prostate Cancer
Richard B. van Breemen, PhDPrincipal InvestigatorUniversity of Illinois at Chicago
1 Previous Clinical Trials
120 Total Patients Enrolled
1 Trials studying Prostate Cancer
120 Patients Enrolled for Prostate Cancer
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I can provide blood and urine samples for testing.I do not have any gastrointestinal diseases or cancer.I haven't taken lycopene supplements in the last 2 weeks.I do not have any prostate disease.
Research Study Groups:
This trial has the following groups:- Group 1: Arm I
- Group 2: Arm II
- Group 3: Arm III
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Prostate Cancer Patient Testimony for trial: Trial Name: NCT00322114 — N/A
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