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Cardioprotective Effect of Melatonin Versus Vitamin D in Breast Cancer Patients Receiving Doxorubicin

Clinical Study Evaluating Cardioprotective Effect of Melatonin Versus Vitamin D in Breast Cancer Patients Receiving Doxorubicin

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07349459
Enrollment
90
Registered
2026-01-16
Start date
2026-04-30
Completion date
2026-08-30
Last updated
2026-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Patients Diagnosed, Doxorubicin, Melatonin, Vitamin D Concentration

Keywords

Vitamin D, Doxorubicin, Cardioprotective Effect, Melatonin, Breast Cancer Patients

Brief summary

This study aims to assess the cardioprotective effect of melatonin and vitamin D in breast cancer patients who receive doxorubicin.

Detailed description

Doxorubicin is one of the most potent chemotherapeutic agents and is widely used for the treatment of various cancers and hematological malignancies . Although Doxorubicin has a potential beneficial effect in cancer treatment, its dose-dependent cardio toxicity is considered a major challenge. Doxorubicin is known to generate free radicals either by redox cycling between a semiquinone form and a quinone form or by forming a Doxorubicin-Fe3+ complex . In both pathways, molecular oxygen is reduced to superoxide ion , which is converted to other forms of reactive oxygen species such as hydrogen peroxide and hydroxyl radical . These free radicals could then cause membrane and macromolecule damage, both of which lead to injury to the heart, an organ that has a relatively low level of antioxidant enzymes such as superoxide dismutase and catalase . Furthermore, it was revealed that Doxorubicin may enhance the death of cardiomyocytes by affecting the tumor necrosis factor signaling pathway via increasing the expression and levels of inflammatory genes interleukin and interleukin -6 . To alleviate DOX-induced toxicity, researchers have tested a number of strategies, including the administration of antioxidants and/or antiapoptotic agents, in both in vitro and in vivo models of Doxorubicin induced cytotoxicity, but most of these trials have failed to translate into clinical benefits . As a result, there are no effective approaches for alleviating Doxorubicin induced cytotoxicity despite intensive research over recent decades . Melatonin is a natural hormone that is primarily secreted by the pineal gland and functions as a major regulator of circadian rhythms in humans . Melatonin also plays a variety of biological roles as a modulator of mood, sexual behavior and sleep; low levels or a deficiency of melatonin are also associated with Parkinson's disease, Alzheimer's disease, epilepsy, ischemic injury, diabetes, and even cancer . Melatonin has emerged as a promising adjuvant that protects against doxorubicin-induced cytotoxicity, as highlighted by various studies and clinical trials that have demonstrated cardioprotective effects against several chemotherapeutic agents . Moreover, melatonin exhibits low toxicity and easily enters cells owing to its good solubility in both aqueous and organic phases and its highly lipophilic properties . Vitamin D plays an important role in the regulation of body function including the cardiovascular system . Vitamin D deficiency results in the decrease of active calcitriol leading to inhibition of proliferation of cardiomyocytes and vascular smooth muscles . This study aims to assess the cardioprotective effect of melatonin and vitamin D in breast cancer patients who receive doxorubicin.

Interventions

DRUGGroup 1 (Doxorubicin group)

30 patients will receive a traditional chemotherapeutic agent (Doxorubicin group) for 12 weeks.

DRUGGroup 2: Vitamin D group

patients with Vitamin D supplementation (1000 iu/day) plus traditional therapy for 12 weeks

DRUGGroup 3: melatonin group

patients with 10 mg of melatonin orally, once daily plus traditional therapy for 12 weeks

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age from 18 to 65 years old. * Gender: female. * Positive breast cancer women who are scheduled to receive Doxorubicin. * Have a good performance status according to the eastern cooperative oncology group with a score of 0-2. * Normal baseline Echocardiography with left ventricular ejection fraction ≥ 50%. * Normal renal and liver function tests.

Exclusion criteria

* Pregnant or breastfeeding women. * Women with HER-2 positive of breast cancer. * Formerly treated with Doxorubicin. * Patients with a known hypersensitivity to any of the used drugs. * On other concomitant vitamins or food supplements. * Valvular heart disease, coronary artery disease, history of congestive heart failure or cardiomyopathy. * Impaired Left ventricular systolic function in which the Left Ventricular Ejection Fraction \< 50%.

Design outcomes

Primary

MeasureTime frameDescription
Decreasing incidence and severity of cardiotoxicity12 weeksAssessment of decreasing incidence and severity of cardiotoxicity by echocardiogram and ejection fraction is associated with doxorubicin treatment.

Secondary

MeasureTime frame
change in the serum level of the (biological markers).12 weeks

Countries

Egypt

Contacts

CONTACTMajed Alharbi, Resident
Ph.majed33@gmail.com+966 55 189 8178

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026