Broccoli compound may shield hearts from chemo damage
NCT ID NCT03934905
First seen Jun 29, 2026 · Last updated Jun 30, 2026 · Updated 1 time
Summary
This trial investigates whether sulforaphane, a nutrient found in broccoli, can reduce heart damage caused by the chemotherapy drug doxorubicin in breast cancer patients. About 70 participants will receive either sulforaphane or a placebo alongside their chemotherapy. The study measures changes in heart function and signs of heart injury to see if the supplement offers protection.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sulforaphane (a nutrient found in broccoli and other cruciferous vegetables)
- What this could lead to
- If it works, this could lead to a simple dietary supplement that helps prevent heart damage from a common chemotherapy drug, improving safety for breast cancer patients.
- What could go wrong
- This is an early-phase trial with only 70 participants, so results may not apply to everyone. The supplement may not protect the heart or could interact with chemotherapy in unexpected ways.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2022
- Expected to finish
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Jun 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 89 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 18 to 89 years 2. No prior diagnosis of coronary artery, carotid artery or peripheral artery disease 3. Not pregnant or breastfeeding (urine pregnancy test will be done if female of childbearing potential) 4. Breast cancer requiring treatment with DOX-containing regimen above 5. Women in child bearing age group (18-50 years) will agree to use birth control for duration of study 6. Study subjects must be willing and able to swallow caplets, up to 8 daily. Exclusion Criteria: 1. Currently on a research study with an investigational drug, or has been on one in the previous 30 days 2. Pregnant (by urine pregnancy test) 3. Baseline ejection fraction of less than 50%, evidence of left ventricular hypertrophy or baseline EKG reported as abnormal per cardiologist. 4. Inability to provide informed consent. 5. Prior history of chest radiation therapy 6. Diabetes or Hypertension or prior Myocardial infarction 7. Trastuzumab patients 8. Routinely taking vegetable or fruit-containing supplement pills (antioxidant phytochemicals) (daily vitamin pills ok) 9. Inability to follow up for safety monitoring 10. Prisoners 11. Previous or current use of cocaine or any illicit drug 12. Unable or unwilling to provide blood samples 13. Taking medications known to have cardiac effects, such as but not limited to, beta blockers, anti-arrhythmic agents, non dihydropyridine calcium channel blockers, ace inhibitors, NSAIDS, diuretic agents. 14. Unable to follow the protocol 15. Inability to receive anthracycline due to any reason (underlying baseline cardiac dysfunction due to other reasons, with an EF under 50%) 16. Patients already taking SFN OTC
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Texas Tech University Health Sciences Center
RECRUITINGLubbock, Texas, 79430, United States
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