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Breast Cancer clinical trials

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NCT ID: NCT01724450 Completed - Breast Cancer Clinical Trials

Carvedilol Effect in Preventing Chemotherapy - Induced Cardiotoxicity

Ceccy
Start date: April 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate if carvedilol can prevent the cardiotoxicity after chemotherapy in breast cancer.

NCT ID: NCT01723592 Completed - Breast Cancer Clinical Trials

Orall Administered Probiotics to Improve the Quality of the Vaginal Flora of Women With Breast Cancer and Chemotherapy.

Start date: October 2012
Phase: N/A
Study type: Interventional

The aim of this study is the improvement of the vaginal flora by at least two grades of the Nugent scale after application of oral probiotics.

NCT ID: NCT01723423 Completed - Breast Cancer Clinical Trials

Mastectomy Reconstruction Outcomes Consortium (MROC) Study

MROC
Start date: August 2011
Phase: N/A
Study type: Observational

The MROC Study seeks to evaluate and compare from the patient's point of view the leading options for breast reconstruction after mastectomy. This study will help patients, physicians, payers and policy makers better understand the various surgeries available for breast reconstruction. Although many women choose reconstruction, the number of options as well as their pros and cons can make decision making difficult and stressful. From this research, we hope to learn more about what works best for patients undergoing these operations.

NCT ID: NCT01722968 Completed - Breast Cancer Clinical Trials

A Biomarker Study in Patients With HER2-negative Metastatic Breast Cancer Treated With Bevacizumab and Paclitaxel

BEVPAC
Start date: November 2012
Phase: Phase 2
Study type: Interventional

To explore molecular biomarkers and/or gene expression signatures that predict response to bevacizumab given in combination with paclitaxel as first line therapy in HER2 negative metastatic breast cancer (MBC).

NCT ID: NCT01722851 Completed - Breast Cancer Clinical Trials

Circulating miRNAs.

Start date: May 2011
Phase:
Study type: Observational

To identify a panel of circulating miRNA markers which could help identify those breast cancer patients who are most likely to respond well to neoadjuvant and adjuvant chemotherapy, and indeed serve as an overall prognostic factor and stratify patients into risk categories which would further guide their management. Similarly, the investigators aim to identify a panel of circulating miRNA markers which could monitor patient's response to chemotherapy and hormonal therapies. Ideally a suitable panel of markers would show significant changes in expression level in good-responders whilst little or no change would be observed in miRNA expression in non-responders.

NCT ID: NCT01719562 Completed - Breast Cancer Clinical Trials

MRI in Detecting Heart Damage in Patients With Cancer Receiving Chemotherapy With Exercise Capacity Addendum

Start date: January 1, 2013
Phase: N/A
Study type: Interventional

This trial studies how well magnetic resonance imaging (MRI) works in detecting heart damage in patients with cancer receiving chemotherapy. Diagnostic procedures, such as MRI, may help doctors predict whether patients will have heart damage caused by chemotherapy in patients with cancer receiving chemotherapy. Exercise Capacity Addendum Brief Summary: This study is designed to demonstrate feasibility of performing the physical activity intervention and the primary outcome measures before, during and six months after initiating Anth-bC for treatment of non- or Hodgkin lymphoma. This study will test the potential for a novel (lifestyle) intervention designed to improve exercise capacity, health-related quality of life and cardiac and cognitive dysfunction. This data will inform the development of the R33 phase of the clinical trial to determine if the physical activity intervention can reduce exercise intolerance in this high-risk population. In addition, cardiac MRI data from individuals within this pilot will be compared to cardiac MRI data from individuals in the parent study that did not undergo either of the two interventional arms of this study.

NCT ID: NCT01717261 Completed - Breast Cancer Clinical Trials

Single Pre-Operative Radiation Therapy (SPORT) for Low Risk Breast Cancer

SPORT
Start date: August 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if partial breast irradiation administered in a single preoperative fraction is tolerable.

NCT ID: NCT01716065 Completed - Breast Cancer Clinical Trials

Regional Anesthesia Versus General Anesthesia on Circulating Tumor Cells (CTC)

CTC
Start date: June 2012
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether the type of anesthesia during breast cancer surgery has any impact on the way a patient's immune system functions for a brief period after surgery. If the investigators find that one type of anesthesia versus the other is more beneficial to a patient's immune system, then the investigators may use this information to design a larger study to exam the effect of anesthesia better.

NCT ID: NCT01712893 Completed - Breast Cancer Clinical Trials

Simultaneous Versus Sequential Use of Adjuvant Chemotherapy and GnRHa in Treating ER+,Premenopausal Breast Cancer

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The present study is a randomized open-label -phase III study that aims to compare the efficacy and safety of the adjuvant chemotherapy with simultaneous or sequential application of Zoladex up to 2-3 years for ≤ 45 year old premenopausal hormone receptor-positive breast cancer.

NCT ID: NCT01711502 Completed - Clinical trials for Breast Cancer Nos Metastatic Recurrent

Epidemiology and Management of Metastatic Breast Cancer

Start date: January 2013
Phase: N/A
Study type: Observational

This is a multicenter, national, retrospective chart-review study that will be based on the collection of data from electronical or paper-based medical records with available data on female patients diagnosed with metastatic brest cancer . The main purpose of this study is to provide accurate, evidence based description on the incidence of progression of metastatic breast cancer and its clinical management.