Clinical Trials Directory

Trials / Completed

CompletedNCT04166253

Protective Role of Vitamin D in Breast Cancer Patients Treated With Doxorubicin

The Potential Protective Effects of Vitamin (D) Against Doxorubicin Induced Cardiotoxicity in Breast Cancer Patients

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Damanhour University · Academic / Other
Sex
Female
Age
30 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The study is aimed at Evaluation of the potential protective effect of Vitamin D in doxorubucin- induced toxicity in breast cancer patients. Proposal Steps: 1. 100 Patients recruited from Alexandria Main University Hospital (AMUH), Oncology Unit are randomly assigned in to two groups: * Control group (n=50) the patient will receive AC regimen (Doxorubucin \& cyclophosphamide) for 4 cycles every 21 day (i.e. 3 months.) * Vitamin D group (n=50) who will receive 4 Cycles AC regimen in addition to vitamin D (Bon One 0.5 microgram®) once daily. 2. Echocardiography (Echo) will be done at base line and at the end of the treatment. 3. Vitamin D, LDH, Troponin-t as well as IL-6 will be assessed at baseline and at the end of the study.

Detailed description

Research Objectives: Evaluation of the potential protective effect of Vitamin D in doxorubucin- induced toxicity in breast cancer patients. Proposal Steps: 1. Assessing breast cancer patients taking part in the study receiving adjuvant chemotherapy AC (Anthracycline (Doxorubucin)-cyclophosphamide) for breast cancer for 4 cycles every 21 day (i.e. 3 months.) 2. 100 Patients are randomly assigned in to two groups: * Control group (n=50) the patient will receive AC regimen (Doxorubucin \& Cyclophosphamide) for 4 cycles every 21 day (i.e. 3 months.) * Vitamin D group (n=50) who will receive 4 Cycles AC regimen in addition to vitamin D once daily. 3. All participants are recruited from AMUH Hospital Oncology Unit. All participants will be given their consent. The study will be approved by research ethics committee of Damanhour University. 4. Tumor staging is done according to American joint committee on cancer (TNM staging of breast cancer eighth edition (Amin et al., 2017). 5. All patients will be submitted to: * Full patient history and clinical examination. * Routine follow up before and after each chemotherapy cycle (complete blood picture, liver function tests, renal function tests. 6. Echocardiography (Echo) at base line and at the end of the treatment. 7. Vitamin D, LDH, Troponin-t as well as IL-6 will be assessed at baseline and at the end of the study. Methodology: Venous blood samples will be analyzed using ELISA Vitamin D, IL-6 kits and immuno-histo-chemistry Troponoin-T and LDH and kits.

Conditions

Interventions

TypeNameDescription
DRUGVitamin DAlfacalcidol oral tablets once daily

Timeline

Start date
2019-09-01
Primary completion
2020-04-01
Completion
2020-05-01
First posted
2019-11-18
Last updated
2021-02-03

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04166253. Inclusion in this directory is not an endorsement.