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Omega-3 Fatty Acids for Preventing Breast Cancer
N/A
Waitlist Available
Research Sponsored by Cedars-Sinai Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Performance status SWOG 0-1
Not eligible for or refused standard breast cancer risk reduction strategies (e.g., prophylactic oophorectomy, prophylactic mastectomy, or tamoxifen)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is testing if omega-3 fatty acids can prevent breast cancer in women who are at high risk of developing it.
Who is the study for?
This trial is for women at high risk of breast cancer due to family history, genetic factors like BRCA mutations, or personal medical history. Participants should have a significant chance of developing breast cancer and not be pregnant or nursing. They must also meet specific health criteria regarding liver, kidney, and blood cell counts.Check my eligibility
What is being tested?
The study is testing the effectiveness of omega-3 fatty acids in preventing the development or recurrence of breast cancer in high-risk women. It's a randomized trial which means participants will be randomly assigned to receive either omega-3 supplements or a placebo for comparison.See study design
What are the potential side effects?
While the side effects are not detailed here, common side effects associated with omega-3 supplements can include fishy aftertaste, upset stomach, and nausea. More serious side effects are rare but could involve bleeding if taken in high doses.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am fully active or restricted in physically strenuous activity but can do light work.
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I have not had, or have chosen not to have, preventive breast cancer surgery or take tamoxifen.
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I am 18 years old or older.
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I haven't had any cancer except for nonmelanoma skin cancer in the last 5 years.
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My recent mammogram showed no signs of cancer.
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I am female.
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
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Breast density as measured by the Madena method at 1 year
Find a Location
Who is running the clinical trial?
Cedars-Sinai Medical CenterLead Sponsor
499 Previous Clinical Trials
164,777 Total Patients Enrolled
16 Trials studying Breast Cancer
2,044 Patients Enrolled for Breast Cancer
Agustin Garcia, MDStudy ChairCedars-Sinai Medical Center
11 Previous Clinical Trials
219 Total Patients Enrolled
2 Trials studying Breast Cancer
100 Patients Enrolled for Breast Cancer
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have not had both breasts removed.I have not had, or have chosen not to have, preventive breast cancer surgery or take tamoxifen.I am 18 years old or older.I haven't had any cancer except for nonmelanoma skin cancer in the last 5 years.My ovarian cancer has been in remission for over 5 years.I haven't had hormonal therapy in the last 6 months.I haven't had cancer treatments that would stop me from joining this study.I haven't taken NSAIDs or COX-2 inhibitors regularly for over 3 months.I am fully active or restricted in physically strenuous activity but can do light work.I don't have any health or social issues that would stop me from joining the study.I have had a non-invasive breast cancer in one breast.I had stage I breast cancer and have completed all standard treatments.I am at high risk for breast cancer due to my genetics or family history.My recent mammogram showed no signs of cancer.I am female.
Research Study Groups:
This trial has the following groups:Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this experiment still open to more participants?
"The clinicaltrials.gov website indicates that this trial, initially posted on April 1st 2005, is not currently calling for participants. Nonetheless, there are presently 2602 other active trials where one can volunteer as a participant."
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