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Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

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NCT ID: NCT00580112 Completed - Breast Neoplasms Clinical Trials

An Efficacy Study of Trabectedin in the Treatment of Participants With Specific Subtypes of Metastatic Breast Cancer

Start date: June 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of trabectedin in 3 subpopulations of participants with previously treated progressive metastatic ( spread of a cancer from one organ or part to another non-adjacent organ or part) breast cancer (abnormal tissue that grows and spreads in the body until it kills) participants.

NCT ID: NCT00579826 Completed - Breast Cancer Clinical Trials

Study of Breast Cancer Prevention by Letrozole in High Risk Women

Start date: October 2006
Phase: Phase 2
Study type: Interventional

This is a multi-institution double-blind placebo-controlled trial whose main objective is to determine if 6 months of letrozole (2.5 mg daily) can reduce proliferation as assessed by Ki-67 in high risk postmenopausal women on systemic hormone replacement therapy who have random periareolar fine needle aspiration (RPFNA) evidence of hyperplasia with atypia or borderline atypia, and a minimum Ki-67 of >1.5%. The primary hypothesis is that proliferation and expression of other estrogen response genes will be favorably modulated by six months of letrozole relative to placebo without substantially increasing hot flashes or worsening overall quality of life.

NCT ID: NCT00579800 Completed - Breast Cancer Clinical Trials

Newer Breast MRI Sequences for the Evaluation of Breast Cancer -FIESTA, Vibrant-DE and IDEAL: Feasibility Evaluation

Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate new computer software on breast magnetic resonance imaging (MRI). The information from this study may help doctors and scientists develop better ways to find breast cancer, and may help future patents with cancer.

NCT ID: NCT00577122 Completed - Clinical trials for Stage IV Breast Cancer

Medroxyprogesterone +/- Cyclophosphamide & Methotrexate in Hormone Receptor-Negative Recurrent/Metastatic Breast Cancer

Start date: July 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the impact of MPA alone and in combination with low dose oral chemotherapy in patients with ER- and PR- advanced breast cancer.

NCT ID: NCT00575354 Completed - Breast Neoplasms Clinical Trials

Comparison of Sevoflurane and Isoflurane Anesthesia for Benign Breast Tumor Excision

CSIABTEC
Start date: March 2007
Phase: Phase 4
Study type: Interventional

Generally, benign breast tumors are excised under the local anesthesia. But such action was so invasive that every patient would experience the physiological and psychological stimuli unavoidably. Sevoflurane was advised as a better inhalational anesthesic for its "easy come,easy go" property during short-lasting operations than isoflurane. We purposed that sevoflurane would be a superior anesthesic for benign breast tumor excision than isoflurane with relative less alteration in hemodynamics, less postoperative side effects and easily-control the depth of anesthesia.

NCT ID: NCT00574587 Completed - Breast Cancer Clinical Trials

Trial for Locally Advanced Breast Cancer Using Vorinostat Plus Chemotherapy

Start date: December 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Vorinostat is a histone deacetylase (HDAC) inhibitor which is approved by the U.S. Food and Drug Administration for the treatment of a rare type of cancer involving the skin (cutaneous T cell lymphoma), but not for breast cancer. HDAC inhibitors work by unsilencing tumor suppressor genes and other genes in the cancer cells that are repressed; when the genes are turned back on by the drug, it leads to death of the cancer cells. HDAC inhibitors such as vorinostat have been shown to enhance the effects of chemotherapy and trastuzumab in experimental systems. The purpose of this trial is to determine the optimal dose of vorinostat to use in combination with standard chemotherapy alone (or in combination with plus trastuzumab for HER2-positive disease), and to determine whether vorinostat enhances the effectiveness of standard chemotherapy (+/- trastuzumab) in patients with locally advanced breast cancer.

NCT ID: NCT00574366 Completed - Breast Cancer Clinical Trials

Erlotinib and Everolimus in Treating Patients With Metastatic Breast Cancer

Start date: December 2005
Phase: Phase 1
Study type: Interventional

RATIONALE: Erlotinib and everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving erlotinib together with everolimus may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of giving erlotinib together with everolimus and to see how well it works in treating patients with metastatic breast cancer.

NCT ID: NCT00574301 Completed - Breast Cancer Clinical Trials

Percutaneous Removal and Margin Ablation for Breast Cancer

Start date: March 2002
Phase: Phase 1/Phase 2
Study type: Interventional

We hypothesize that radiofrequency ablation after single-insertion image guided vacuum assisted biopsy (IVEB) can be used to achieve negative margins in small unicentric breast cancers (≤1.5 cm).

NCT ID: NCT00574145 Completed - Breast Cancer Clinical Trials

Healing Touch in Treating Fatigue in Women Undergoing Radiation Therapy for Breast Cancer

Start date: February 2007
Phase: N/A
Study type: Interventional

RATIONALE: Healing touch therapy may be effective in lessening fatigue in women with breast cancer who are undergoing radiation therapy. PURPOSE: This randomized clinical trial is studying how well healing touch works in treating fatigue in women undergoing radiation therapy for breast cancer.

NCT ID: NCT00573495 Completed - Breast Cancer Clinical Trials

Multipeptide Vaccine for Advanced Breast Cancer

Start date: November 2007
Phase: Phase 1
Study type: Interventional

This is a study on how to activate the immune system with a vaccine. The vaccine is made up of two proteins found in breast cancer: telomerase and survivin. The vaccine is given in combination with other drugs that may also have an effect on the immune system and attack the cancer. The goals of the study are: 1. to test the safety of the combination of agents 2. to find out what effects the treatment has on advanced breast cancer