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Breast Cancer clinical trials

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NCT ID: NCT00556218 Completed - Breast Cancer Clinical Trials

Meditation and Cognitive Function in Women With Breast Cancer

Start date: October 24, 2007
Phase: N/A
Study type: Interventional

The goal of this behavioral research study is to learn if participating in a Tibetan meditation program helps to improve quality of life for women after chemotherapy and during recovery from breast cancer. Whether the meditation program helps to improve brain function and sleep quality will also be studied.

NCT ID: NCT00555386 Completed - Breast Cancer Risk Clinical Trials

Soy, Selenium and Breast Cancer Risk

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

There is evidence to suggest that some dietary components can reduce the risk of breast cancer. In this pilot study two such components, isoflavones (compounds found in soy products) and selenium, will be given to women classed as at moderate to high risk of the disease. The aim is to determine some novel biomarkers of risk and to see the effect of supplementation on them.

NCT ID: NCT00553410 Completed - Breast Cancer Clinical Trials

Letrozole in Preventing Cancer in Postmenopausal Women Who Have Received 4-6 Years of Hormone Therapy for Hormone Receptor-Positive, Lymph Node-Positive, Early-Stage Breast Cancer

SOLE
Start date: August 2007
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 more effective in postmenopausal women who have received hormone therapy for early-stage breast cancer. PURPOSE: This randomized phase III trial is comparing two different regimens of letrozole in preventing cancer in postmenopausal women who have received 4-6 years of hormone therapy for hormone receptor-positive, lymph node-positive, early-stage breast cancer.

NCT ID: NCT00551278 Completed - Breast Cancer Clinical Trials

Validation Study Using the GeneSearch BLN Assay to Test Sentinel Lymph Nodes From Patients With Breast Cancer

Start date: October 2007
Phase: N/A
Study type: Observational

The purpose of this trial is to show adequate assay performance on clinical samples tested in real time at the clinical site.

NCT ID: NCT00550134 Completed - Breast Cancer Clinical Trials

Cognitive Changes Associated With Breast Cancer Treatment

Start date: October 24, 2007
Phase:
Study type: Observational

Patients with cancer often complain that their "mind does not seem to be clear." This can be due to stress, depression, anxiety, or physical problems caused by cancer or the treatments used to control symptoms. There are many purposes for this study; one of them is to learn about the effects of cancer treatments on the brain, and another is to identify useful tools to detect these effects. The results of this study may stimulate new research comparing different treatments to the current treatment so the researchers may learn how to treat symptoms more effectively and improve patient quality of life. We would also like to learn more about the effects chemotherapy may have on DNA.

NCT ID: NCT00549822 Completed - Breast Cancer Clinical Trials

Intermittent Letrozole Therapy in Postmenopausal Women With Metastatic Breast Cancer

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

The purpose of this research study is to study the effects of using aromatase inhibitor (AI) therapy intermittently on participants with breast cancer. AIs are a class of drugs used to treat breast cancer in postmenopausal women. They work by decreasing the level of estrogen, which is believed to stimulate the growth of tumor tissue. Breast cancer that progresses despite therapy with an AI is thought to have become resistant to AI therapy. There is scientific evidence to suggest that resistant breast cancer cells learn to grow at the very low levels of estrogen present on AI therapy, and that increasing estrogen levels even slightly by stopping AI therapy may inhibit the breast cancer cells.

NCT ID: NCT00548899 Completed - Breast Cancer Clinical Trials

Neoadjuvant Chemotherapy Including Sorafenib in Women With Previously Untreated Primary Breast Cancer

SOFIA
Start date: November 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of sorafenib in the neoadjuvant setting in patients with primary breast cancer

NCT ID: NCT00548392 Completed - Breast Cancer Clinical Trials

Sonographic Visibility of Breast Biopsy Marker Clips Up to 4 Weeks After Placement

Start date: May 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine how long collagen based marker clips remain visible by ultrasound after placement in suspicious breast lesions and if collagen based marker clips can be reliably identified in the operating room and serve as effective guidance for surgical removal of high risk or malignant breast lesions.

NCT ID: NCT00548184 Completed - Breast Cancer Clinical Trials

Lapatinib and Trastuzumab With or Without Endocrine Therapy

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

We think that lapatinib will help to shrink your tumor when given prior to the main or primary therapy for the kind of breast cancer you have been diagnosed with. When treatment is given before the main or primary therapy, it is called neoadjuvant therapy. We will compare lapatinib with lapatinib plus trastuzumab (herceptin) for 12 weeks. If your tumor is estrogen receptor positive (ER positive), estrogen deprivation will also be given to you. Tumors that are ER positive have a lot of estrogen receptors found in them. This is also called "over expression" or amplification of estrogen receptors. The most important information we will get from this study is to see the response to "neoadjuvant" (treatment given before the main treatment), lapatinib with trastuzumab (herceptin) in your tumor tissue sample.

NCT ID: NCT00547989 Completed - Breast Cancer Clinical Trials

Paravertebral Block, an Adjunct to General Anaesthesia for Breast Surgery?

Start date: October 2006
Phase: Phase 3
Study type: Interventional

Aim is to study if a paravertebral block as an adjunct to general anesthesia is a suitable technique for extended, one sided, breast surgery.