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Breast Cancer clinical trials

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NCT ID: NCT00736970 Completed - Breast Cancer Clinical Trials

Oral Deforolimus With Trastuzumab for Patients With HER2-positive Trastuzumab-Refractory Metastatic Breast Cancer (8669-009)

Start date: July 2008
Phase: Phase 2
Study type: Interventional

This clinical trial will study the use of ridaforolimus in metastatic breast cancer subjects whose tumors have shown a resistance to trastuzumab (herceptin). The goal of this study is to find out if subjects treated with ridaforolimus in combination with trastuzumab have a positive response to the treatment, and if treatment with ridaforolimus in combination with trastuzumab prolongs survival.

NCT ID: NCT00735150 Completed - Breast Cancer Clinical Trials

Awareness and Attitudes Regarding Prenatal and Preimplantation Genetic Diagnosis for Inherited Breast/Ovarian Cancer Risk

Start date: March 2008
Phase: N/A
Study type: Observational

We are inviting you to participate in a study of how people who have had genetic counseling for breast/ovarian cancer risk feel about certain reproductive technologies, preimplantation genetic diagnosis (PGD) and prenatal genetic diagnosis (PND), that may reduce the chances of passing increased risk onto one's children. We would also like feedback from patients who have been to our clinic in the past on the best ways to talk about PGD and PND during genetic counseling sessions. We are seeking both the opinions of people who are interested in these technologies and those who are not. It does not matter whether you have heard of PGD or PND before - you can still participate. Your past experience with genetic counseling is valuable to us in deciding how to communicate this information during sessions.

NCT ID: NCT00734955 Completed - Breast Cancer Clinical Trials

An Optical Assay System for Intra Operative Assessment of Tumor Margins in Patients

Start date: May 2006
Phase: N/A
Study type: Interventional

Our objective is to develop a novel optical assay system for intra operative assessment of tumor margins in partial mastectomy or mastectomy specimens. Our group has previously shown that optical techniques can effectively discriminate between malignant and non-malignant breast tissues. We have also shown that data collection and processing from a single point on the tissue specimen requires less than 5 seconds. In addition, the technique is easily adaptable to provide sensing depths that are required for breast margin assessment. The goal of the work proposed in this protocol is to test the sensitivity and specificity of an optical assay system developed by our group, for intra operative assessment of breast tumor margins.

NCT ID: NCT00734838 Completed - Breast Cancer Clinical Trials

Optical Spectroscopy During Breast Cancer Surgery and Core Needle Biopsy

Start date: January 2006
Phase: N/A
Study type: Interventional

The objective of the proposed research is to develop new diagnostic modalities based on optical spectroscopy (auto fluorescence, absorption, and scattering) for the diagnosis of breast cancer and test its performance as an adjunct to core needle biopsy. For the surgery part of the study, all patients scheduled to have a mastectomy or lumpectomy for the treatment of breast cancer will be asked if they would be willing to participate in this study. For the core needle biopsy part of the study, patients with a higher pre-probability of cancer (based on mammography) will be recruited to increase the number of patients with malignant lesions and enrolled in this investigation.

NCT ID: NCT00732056 Completed - Breast Cancer Clinical Trials

A Study of GRN163L With Paclitaxel and Bevacizumab to Treat Patients With Locally Recurrent Or Metastatic Breast Cancer

Start date: July 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose (MTD) of GRN163L in combination with paclitaxel and bevacizumab in patients with locally recurrent or metastatic breast cancer (MBC)

NCT ID: NCT00728442 Completed - Breast Cancer Clinical Trials

Impact of OncoDoc2 on Guideline Compliance in the Management of Breast Cancer

OncoDoc2
Start date: December 2008
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate how the use of OncoDoc2, a computerized guideline-based decision support system, could improve the compliance of multidisciplinary staff meeting decisions with local clinical practice guidelines in the management of non-metastatic breast cancer.

NCT ID: NCT00727948 Completed - Breast Cancer Clinical Trials

The Effect of Aspirin on Angiogenesis Proteins in Women on Tamoxifen Therapy

Start date: July 2008
Phase: Early Phase 1
Study type: Interventional

Changes in major angiogenic proteins have been seen following initiation of tamoxifen and aromatase inhibitor therapy in women with breast cancer. One source of these proteins is the circulating platelet pool. The investigators hypothesize that in addition to their anti-platelet properties, agents such as aspirin can be used as targeted anti-angiogenesis therapy. The investigators will determine the influence of aspirin on the release of angiogenic proteins from platelets in 35 patients with breast cancer.

NCT ID: NCT00727883 Completed - Breast Cancer Clinical Trials

Retrospective Observational Trial on Reasons for Withdraw of Adjuvant Tamoxifen in Breast Cancer Patients

SOSTA
Start date: July 2007
Phase: N/A
Study type: Observational

Retrospective observational trial on reasons for withdraw of Adjuvant Tamoxifen in Breast Cancer patients

NCT ID: NCT00727662 Completed - Breast Cancer Clinical Trials

A Yoga and Wellness Program for Breast Cancer Survivors With Persistent Fatigue

Start date: June 2008
Phase: N/A
Study type: Interventional

This randomized controlled trial will compare the effectiveness of an Iyengar Yoga intervention to a Wellness Seminar health education lecture series, for improvements in energy, mood and biological functioning in breast cancer survivors with persistent, post-treatment fatigue. It is anticipated that the Iyengar Yoga intervention will be feasible and acceptable to breast cancer survivors with minimal side effects and that the Yoga intervention will be effective in improving fatigue and physical performance.

NCT ID: NCT00726661 Completed - Breast Cancer Clinical Trials

An Observational Study of Treatment Patterns and Safety Outcomes for Metastatic or Locally Recurrent Breast Cancer (VIRGO)

VIRGO
Start date: June 2008
Phase: Phase 4
Study type: Observational

This is a multicenter, prospective OCS designed to follow patients with locally recurrent or metastatic breast cancer in the United States. Two cohorts will be included: - Patients with HER2-negative disease receiving their first cytotoxic chemotherapy and/or targeted therapy (approximately 825 patients) - Patients with HR-positive disease receiving their first HT for advanced disease (approximately 425 patients) Patients who have received any chemotherapy for advanced disease more than 8 weeks prior to enrollment to this OCS will not be eligible. A total of approximately 1,250 patients will be enrolled. Approximately 150 study sites will be activated in order to achieve complete enrollment by December 2010.