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Breast Cancer clinical trials

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NCT ID: NCT03885648 Active, not recruiting - Breast Cancer Clinical Trials

Breast Cancer and Its Relationship With the Microbiota

MICROMA
Start date: January 1, 2018
Phase:
Study type: Observational

Breast cancer ranks first in women, and is the second cause of death in this gender. In addition to genetics, the environment contributes to the development of the disease, although the factors involved are not well known. Among the latter is the influence of microorganisms and, therefore, attention is recently being paid to the mammary microbiota. The hypothesis of this study is that the risk of breast cancer could be associated with the composition and functionality of the mammary/gut microbiota, and that exposure to environmental contaminants (endocrine disruptors, EDCs) might contribute to alter the microbiota. This is a case-control clinical study that will be performed in women between 25 and 70 years of age. Cases will be women diagnosed and surgically intervened of breast cancer (stages I and II). Women with antecedents of cancer or advanced tumor stage (metastasis), or who have received antibiotic treatment within 3 months prior to recruitment, or any neoadjuvant therapy, will be excluded. Controls will be women surgically intervened of breast augmentation or reduction. Women with oncological, gynecological or endocrine history, and those who have received antibiotic treatment within 3 months prior to recruitment will also be excluded. Blood, urine, breast tissue and stool samples will be collected. Data regarding anthropometric, sociodemographic, reproductive history, tumor features and dietary habits will be gathered. Metabolomic studies will be carried out in stool and breast tissue samples. Metagenomic studies will also be performed in stool and breast tissue samples to ascertain the viral, fungal, bacterial and archaea populations of the microbiota. Quantitation of estrogens, estrogen metabolites and EDCs in samples of serum, urine and breast tissue will also be performed. This is the first time that the contribution of bacteria, archaea, viruses and fungi together with their alteration by environmental contaminants to the risk of breast cancer will be evaluated in the same study. Results obtained could contribute to elucidate risk factors, improve the prognosis, as well as to propose novel intervention studies in this disease.

NCT ID: NCT03878017 Active, not recruiting - Clinical trials for Breast Cancer Female

A Novel Method of Clipped Axillary Lymph Node Localization Post Neoadjuvant Chemotherapy in Breast Cancer Patients .

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

to determine the feasibility of a novel technique of localization of clipped LN post neoadjuvant chemotherapy

NCT ID: NCT03872908 Active, not recruiting - Breast Cancer Clinical Trials

Satisfaction & Efficacy of Compression Using Surgical Gloves in Chemo-induced Peripheral Neuropathies

ELEGANT
Start date: September 29, 2019
Phase:
Study type: Observational

Evaluation of Satisfaction & Efficacy of Compression Using Surgical Gloves in Peripheral Neuropathies Due to Chemotherapy

NCT ID: NCT03870919 Active, not recruiting - Surgery Clinical Trials

Locoregional Treatment and Palbociclib in de Novo, Treatment Naive, Stage IV ER+, HER2- Breast Cancer Patients

PALATINE
Start date: October 23, 2019
Phase: N/A
Study type: Interventional

Approximately 3.5% to 6% of newly diagnosed breast cancer patients are stage IV metastatic. De novo metastatic breast cancer accounts for 20% to 25% of these cases. Despite a decrease in mortality in Europe and North America due to early detection and access to treatment, breast cancer remains the 2ⁿᵈ leading cause of cancer deaths in developed countries after lung cancer and the world's leading cause. In the ESME French national retrospective cohort (NCT03275311), the newly diagnosed estrogen receptor (ER)-positive and HER2-negative (luminal) metastatic patients had a 59.1 months overall survival (OS) for pre-menopausal women and 44.7 months for postmenopausal women. In the same cohort, the median OS was 47.4 months for de novo metastatic patients with hormone receptor (HR)-positive / HER2-negative breast cancer. The most important current treatment for metastatic breast cancer remains systemic therapy. Surgery and radiation are mainly used to treat symptoms. However, more than 15 retrospective studies have assessed the impact of locoregional treatment on relapse and OS. These studies suggested an improvement of the OS in patients with de novo metastatic breast cancer thanks to the addition of locoregional treatment to systemic therapy. Recent data from the ESME cohort suggest that patients with de novo luminal or HER2-positive metastatic breast cancer may benefit from local treatment of the primary tumor. Several prospective trials have attempted to demonstrate the benefit of locoregional treatment with mixed results. This can be explained by a limited power of statistical analysis, on the recruitment of patients with breast cancer of all types, and on a limited access to effective systemic therapies in some cases and all before the area of anti CD4/6 which is the current standard treatment in patients with HR-positive / HER2-negative luminal metastatic disease. However, guidelines indicate that a "multimodal approach, including curative locoregional treatments, should be considered". As a result, many clinicians offer locoregional treatment of the primary tumor, especially if there is a good response to the first line of systematic treatment. Taken together, these data underscore the need for an evaluation of the value of combined therapy - endocrine therapy - CDK4/6 inhibitor and locoregional treatment - in this population of patients with newly diagnosed HR-positive / HER2-negative breast cancer.

NCT ID: NCT03866655 Active, not recruiting - Breast Cancer Clinical Trials

Evaluating a Digital Tool for Supporting Breast Cancer Patients

ADAPT
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

This is a prospective randomised controlled trial that aims to understand the impact of the OWise breast cancer digital tool in newly diagnosed breast cancer patients. Half the patients will receive the digital tool and half the patients will receive standard information. The study will look at the impact of the digital tool on patient activation, health related quality of life (HRQoL), health status, psychological distress, NHS resource utilisation and health care costs.

NCT ID: NCT03865992 Active, not recruiting - Breast Cancer Clinical Trials

Curcumin in Reducing Joint Pain in Breast Cancer Survivors With Aromatase Inhibitor-Induced Joint Disease

Start date: March 4, 2019
Phase: N/A
Study type: Interventional

This phase I trial studies how well curcumin works in reducing joint pain in patients who are breast cancer survivors and have joint disease caused by treatment with aromatase inhibitors. Curcumin is an ingredient of turmeric, a plant in the ginger family, which is commonly used in curries and South Asian and Middle Eastern cooking, and may decrease joint pain in patients with arthritis from other conditions (such as osteoarthritis and rheumatoid arthritis).

NCT ID: NCT03862131 Active, not recruiting - Breast Cancer Clinical Trials

PROactive Evaluation of Function to Avoid CardioToxicity

PROACT
Start date: March 13, 2019
Phase: Phase 2
Study type: Interventional

This study is intended to evaluate the ability of an intramyocardial strain analysis package with cardiac MRI to assist in the early detection and management of cardiotoxicity from therapeutics used to treat cancer.

NCT ID: NCT03859453 Active, not recruiting - Breast Cancer Clinical Trials

Follow-up in Early and Locally Advanced Breast Cancer Patients

Start date: October 14, 2020
Phase:
Study type: Observational

A cross-sectional follow-up study of Early and Locally Advanced Breast Cancer patients after primary treatment.

NCT ID: NCT03858322 Active, not recruiting - Breast Cancer Clinical Trials

'ADVANCE' (A Pilot Trial)

Start date: March 21, 2019
Phase: Phase 1
Study type: Interventional

This study is being conducted to carefully study how chemotherapy is tolerated in group of patients age 70.

NCT ID: NCT03847623 Active, not recruiting - Breast Cancer Clinical Trials

Effect of Preoperative Curcumin in Breast Cancer Patients

EPC
Start date: June 18, 2017
Phase: N/A
Study type: Interventional

Effect of curcumin on modulation of immune and inflammatory parameters in pre-operative patients