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Breast Neoplasms clinical trials

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NCT ID: NCT01067989 Terminated - Chemotherapy Clinical Trials

Low-Dose/Metronomic(LDM)Chemotherapy for Metastatic Breast Cancer

Start date: March 2010
Phase: Phase 2
Study type: Interventional

Low-dose metronomic(LDM)chemotherapy as well as anti-inflammatory agents and bisphosphonates have shown anti-angiogenic properties on tumor vasculature. This study is meant to test the therapeutic potential of an anti-angiogenic treatment strategy by combining all these agents for metastatic breast cancer patients.

NCT ID: NCT01067976 Completed - Breast Cancer Clinical Trials

Efficacy and Safety of Gadobutrol 1.0 Molar (Gadovist) for Breast MRI

Start date: February 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to look at the efficacy (how does it work) and safety of gadobutrol when used for obtaining MR images of both breasts.Women with a recent diagnosis of breast cancer by mammogram (X-ray examination of the breasts) may benefit from MRI of the breasts as MRI may detect additional breast cancers.

NCT ID: NCT01064635 Active, not recruiting - Breast Cancer Clinical Trials

Letrozole in Treating Breast Cancer in Postmenopausal Women With Stage I, II, or III Breast Cancer Previously Treated With Tamoxifen (GIM4)

GIM4
Start date: August 2005
Phase: Phase 3
Study type: Interventional

RATIONALE: Estrogen can cause the growth of breast cancer cells. Letrozole may fight breast cancer by lowering the amount of estrogen the body makes. It is not yet known which regimen of letrozole is most effective in treating breast cancer in postmenopausal women who have received tamoxifen. PURPOSE: This randomized phase III trial is comparing different regimens of letrozole to see how well they work in treating postmenopausal women with stage I, stage II, or stage III breast cancer previously treated with tamoxifen.

NCT ID: NCT01064427 Recruiting - Clinical trials for Newly Diagnosed Breast Cancer

Factors Correlated With Fatigue in Breast Cancer

FATSEIN
Start date: July 2008
Phase: N/A
Study type: Observational

The aim of this study is to identify the determinants of cancer-related fatigue, and the long-term effect of the different adjuvants treatments will be explored. A prospective longitudinal study in women diagnosed for the first time with stage I-III breast cancer and who have undergone surgery, has been designed to meet the study aims.

NCT ID: NCT01064349 Completed - Cancer Clinical Trials

Breast Cancer With Over-expression of erbB2-BRAINSTORM

Start date: May 6, 2009
Phase:
Study type: Observational

This retrospective cohort study aims to improve our understanding of the current paradigm for treatment of brain metastases in erbB2+ breast cancer patients in the Asia Pacific region. We aim to identify approximately 300 erbB2+ breast cancer patients with brain metastases diagnosed between 2006-2008 in 6 countries. Medical records will be analyzed to determine the treatment pattern for brain metastases, including anti-erbB2 therapy. Additional objectives are to understand the impact of anti-erbB2 therapy on survival after brain metastases and to investigate the relationship between anti-erbB2 therapy for brain metastases and: 1) the time interval between diagnosis of erb2+ breast cancer and brain metastasis, and 2) the occurrence of brain metastasis as the first site of disease progression.

NCT ID: NCT01061359 Completed - Breast Neoplasm Clinical Trials

Application Of Epirubicin Within A Neo-/Adjuvant Chemotherapy In Patients With Primary Breast Cancer

Start date: January 1999
Phase: N/A
Study type: Observational

Evaluation of efficacy of treatment with epirubicin (5 years follow-up). Evaluation of frequency of dose reduction. Evaluation of frequency of neoadjuvant treatment with E(120mg) / C(600mg). Evaluation of unexpected and serious adverse events. (E=Epirubicin; C =Cyclophosphamide)

NCT ID: NCT01060514 Terminated - Clinical trials for Metastatic Breast Cancer

Pazopanib + Vinorelbine in Non Small Cell Lung Cancer (NSCLC) and Breast Cancer

Start date: February 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the highest dose of Vinorelbine and Pazopanib that can be given together without causing severe side effects. Also, this study will evaluate what effects (good and bad) that the treatment has on patients and their cancer.

NCT ID: NCT01060085 Completed - Clinical trials for Invasive Breast Cancer

Digital Breast Tomosynthesis Versus Contrast Enhanced Magnetic Resonance Imaging (MRI) for Breast Cancer Staging

Start date: February 2009
Phase: N/A
Study type: Observational

The primary objective of this study is to compare the diagnostic accuracy of Digital Breast Tomosynthesis (DBT) versus that of Contrast Enhanced Magnetic Resonance Imaging (CEMRI) in determining the size of breast cancer preoperatively. Secondary objectives include: 1. Comparing the operating characteristics of each combined imaging protocol with respect to the reference standard, i.e. histopathologic assessment, of additional non-index lesions. 2. Comparison of re-excision rates based on estimated disease extent from adjunctive CEMRI vs. adjunctive DBT. 3. Evaluation of patient satisfaction with regard to the adjunctive modality (DBT vs. CEMRI).

NCT ID: NCT01057069 Active, not recruiting - Breast Cancer Clinical Trials

Neo Adjuvant Chemotherapy in Triple Negative Breast Cancer

neo-TN
Start date: January 2010
Phase: Phase 2/Phase 3
Study type: Interventional

This study aims to compare the response of triple-negative breast cancer with deficient homologous recombination to intensified alkylating chemotherapy versus standard chemotherapy with dose dense AC and/or Docetaxel-Capecitabine.

NCT ID: NCT01056757 Terminated - Clinical trials for Metastatic Breast Cancer

Treatment With Ribavirin for Patients With Metastatic Breast Cancer

Start date: December 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to learn whether oral Ribavirin is safe and effective in treating patients with metastatic breast cancer, that have high levels of eIF4E.