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Breast Cancer clinical trials

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NCT ID: NCT02831530 Completed - Breast Cancer Clinical Trials

Randomized Short-term Pre-surgical Study to Assess the Effects of Abemaciclib (LY2835219) in Early Breast Cancer Patients

ABC-POP
Start date: March 16, 2016
Phase: Phase 2
Study type: Interventional

Cyclins CDK4 / 6 are extensively involved in the proliferation and growth of numerous cancers including breast cancer. The objective of this study is to identify if a new preoperative oral treatment, abemaciclib directed against the CDK / 6 compared to no treatment, inhibits tumor growth or induced senescence (aging) tumor. This early study is offered to women who are going to be operated on for breast cancer with expression of hormone receptor (ER and / or PR). These women will have 3 chances to receive one for up to 14 days in the waiting period of their surgery abemaciclib as tablets. Other patients do not receive treatment. The decision to receive or no treatment will be done by a random computer draw. The drug's effectiveness will be evaluated primarily on the biological parameters of the tumor itself when comparing surgery to before treatment. These results biomarkers will allow us to better know how this treatment and eventually will be used in future to identify patients for whom treatment with abemaciclib more efficiency. Patients treated in the protocol will then receive treatment entirely conventional in their breast cancer within the parameters of their tumors: their participation is very limited in time.

NCT ID: NCT02831439 Completed - Breast Cancer Clinical Trials

A Statewide Intervention to Reduce Use of Unproven or Ineffective Breast Cancer Care

Start date: September 2014
Phase: N/A
Study type: Interventional

The goal of this project is to examine the effectiveness and potential cost savings of two organizational interventions aimed at reducing the use of ineffective or unproven care among women with incident breast cancer.

NCT ID: NCT02830282 Completed - Breast Cancer Clinical Trials

Surveillance Markers of Utility for Recurrence After Neoadjuvant Chemotherapy for Breast Cancer

Start date: July 2013
Phase:
Study type: Observational

This is a nested multicenter, prospective cohort study within the I-SPY 2 TRIAL for women undergoing neoadjuvant chemotherapy for primary breast cancer who are also undergoing definitive surgical resection and have clinical or radiographic evidence of residual tumor at the completion of chemotherapy.

NCT ID: NCT02829905 Completed - Breast Cancer Clinical Trials

Women's Experiences of Mammography: Quantitative Evaluation

WEM-Quant
Start date: November 30, 2016
Phase:
Study type: Observational

Study will develop, validate and pilot measures to assess quality of experiences of mammography. Pilot data collection and analysis will investigate modifiable factors most important in determining quality of patient experiences of mammography.

NCT ID: NCT02829021 Completed - Breast Cancer Clinical Trials

Dynamic Infrared Thermography in Breast Cancer Diagnostics

Start date: April 2009
Phase: N/A
Study type: Interventional

This study evaluate diagnostic accuracy of dynamic infrared thermography compared to mammography (reference test) in breast cancer diagnostics. Women aged 50-70 years, selected for assessment after mammography screening were invited to dynamic infrared thermography before clinical mammography and further examination.

NCT ID: NCT02828189 Completed - Breast Cancer Clinical Trials

Therapeutic Exercise in Cancer-Related Fatigue in Women After Breast Cancer Treatment

Start date: July 2016
Phase: N/A
Study type: Interventional

The main objective of this study is to determine whether the proposed program of therapeutic exercise is effective in improving fatigue, more than the exercise unsupervised depending on their preferences, in women treated for breast cancer.

NCT ID: NCT02827370 Completed - Breast Carcinoma Clinical Trials

CAREFOR: Precision Medicine Driving Precision Nutrition for the Treatment of NeoAdjuvant Breast Cancer

Start date: June 16, 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if a targeted dietary change can enhance the effect of neo-adjuvant chemotherapy

NCT ID: NCT02826369 Completed - Breast Cancer Clinical Trials

Use of Compressed Sensing in Breast MRI

COMPRIM
Start date: March 29, 2016
Phase: N/A
Study type: Interventional

Breast MRI is increasingly important in breast screening imaging. It is currently based on dynamic sequences after contrast injection whose temporal resolution must be less than 90 seconds with dynamic acquisitions at different times. These curves profiles are designed to differentiate benign from malignant lesions. Recently, Mann et al, (2014) showed that increasing the temporal resolution of dynamic acquisitions; lesion enhancement curves over time were more accurate than the curves usually performed. It seems necessary to work on sequences having better temporal resolution without compromising however spatial resolution.

NCT ID: NCT02820961 Completed - Breast Cancer Clinical Trials

Drug-Drug Interaction Study of Entinostat and Exemestane in Postmenopausal Women With ER+ Breast Cancer

Start date: June 29, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effect of exemestane on the pharmacokinetics (PK) of entinostat and to determine the effect of entinostat on the PK of exemestane in patients with locally recurrent or metastatic estrogen receptor positive (ER+) breast cancer. Additionally, this study will evaluate the safety and tolerability of entinostat in combination with exemestane, and assess the effectiveness of entinostat in combination with exemestane in terms of best overall response and overall survival.

NCT ID: NCT02815852 Completed - Clinical trials for Breast Cancer in Women Under 40 Years Old

RETROSPECTIVE ANALYSIS OF BREAST BIOPSIES IN WOMEN YOUNGER THAN 40 YEARS OLD

RAD2016
Start date: December 2016
Phase:
Study type: Observational

The purpose of this study is to review retrospectively cases of breast cancer of the centers belonging to the BREST UNIT Tuscany North-West Wide Area and compare the imaging characteristics (ultrasound, mammography and mammary MRI if available) of breast cancer with the corresponding histological reports and assess whether in women <40 years the typical imaging presentation pattern of malignancies observed in women> 40 years are confirmed.