This clinical trial is focused on studying the effects of the medication dapagliflozin on preventing heart damage in patients with breast cancer who are receiving a type of chemotherapy known as anthracycline-based chemotherapy. The study involves patients with invasive breast cancer at stages I to III who are scheduled to start this chemotherapy within 60 days. The medication being tested is called Forxiga, which contains dapagliflozin, and it is compared to a placebo, which looks like the real medication but does not contain the active ingredient.
The purpose of the study is to see if dapagliflozin can help prevent heart problems that might occur as a side effect of the chemotherapy. Participants in the study will be randomly assigned to receive either dapagliflozin or the placebo. The study is designed to be “double-blind,” meaning neither the participants nor the researchers will know who is receiving the actual medication and who is receiving the placebo. This helps ensure that the results are not biased. The study will last for 12 months, during which time the participants’ heart health will be monitored to check for any signs of heart dysfunction, such as changes in heart function or structure, or changes in certain heart-related biomarkers.
Throughout the study, the participants’ heart health will be assessed at different points, including at 6 and 12 months, to see if there are any changes in heart function or symptoms of heart failure. The study will also look at other health outcomes, such as changes in quality of life and any side effects that may occur. The goal is to determine if dapagliflozin can effectively reduce the risk of heart problems in breast cancer patients undergoing anthracycline-based chemotherapy.



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