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Breast Cancer clinical trials

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NCT ID: NCT00918892 Completed - Breast Cancer Clinical Trials

Assessment of Candidate Protein Expression in Breast Cancer Specimens

Start date: January 1, 2011
Phase:
Study type: Observational

RATIONALE: Studying the genes expressed in samples of tumor tissue from patients with cancer may help doctors identify biomarkers related to cancer. PURPOSE: This research study is looking at tumor tissue samples from patients who have undergone surgery for breast cancer.

NCT ID: NCT00918788 Completed - Breast Cancer Clinical Trials

Laser Spectroscopy of Breast Tissue Through a Needle Device

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

RATIONALE: Collecting and storing samples of breast tissue from patients who have undergone biopsy or surgery to test in the laboratory may help the study of cancer in the future. PURPOSE: This laboratory study is looking at samples of breast tissue from women who have undergone breast biopsy or surgery.

NCT ID: NCT00918281 Completed - Breast Cancer Clinical Trials

Reproducibility of 18F Uptake by Solid Tumors Using PET Imaging Following Intravenous Administration of (18F) Injection

Start date: June 2009
Phase: Phase 2
Study type: Interventional

Study aimed to assess the reproducibility of PET imaging using AH111585 (18F) Injection. Subjects are evaluable if they undergo 2 administrations of AH111585 (18F) Injection (3 to 8 days apart) and the corresponding PET acquisitions, and tumors demonstrate detectable levels of 18F uptake on PET.

NCT ID: NCT00918216 Completed - Breast Cancer Clinical Trials

Spectroscopy of Breast Tissue

Start date: March 2008
Phase: Phase 1
Study type: Observational

RATIONALE: Diagnostic procedures, such as laser spectroscopy, may help find and diagnose breast cancer. PURPOSE: This phase I trial is studying laser spectroscopy to see how well it works in diagnosing breast cancer in women with breast lesions.

NCT ID: NCT00917748 Completed - Breast Cancer Clinical Trials

Study With Modafinil in Patients Treated With Docetaxel-Based Chemotherapy for Metastatic Breast or Prostate Cancer (MOTIF)

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

The primary objective is: - To determine the efficacy of modafinil in the reduction of fatigue in patients with metastatic breast or prostate cancer undergoing docetaxel-based chemotherapy The secondary objectives are: - To determine the effect of modafinil on quality of life (QoL) during docetaxel-based chemotherapy - To determine the effect of modafinil on patients physical activity level, functional status, number of chemotherapy cycles tolerated, sleep disturbance and depression, during docetaxel-based chemotherapy - To investigate the impact of tumour type, patient physical activity level, functional status, sleep disturbance and depression on the efficacy of modafinil at improving fatigue and quality of life during docetaxel-based chemotherapy. - To determine the safety and tolerability of modafinil during docetaxel-based chemotherapy

NCT ID: NCT00917735 Completed - Breast Cancer Clinical Trials

Green Tea and Reduction of Breast Cancer Risk

Start date: July 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: Green tea extract contains ingredients (catechins) that may lower the risk of breast cancer. PURPOSE: This phase II trial is studying how well green tea extract works in preventing breast cancer compared to a placebo in postmenopausal women with high breast density. The investigators have hypothesized that green tea consumption reduces breast cancer risk, and this effect is seen primarily in women who have the low-activity COMT genotype. The investigators will test this by evaluating the effects of green tea extract on breast cancer biomarkers including mammographic density, plasma insulin-like growth factor 1 (IGF-1), IGF binding protein 3 (IGFBP-3), estrone, estradiol, androstenedione, sex hormone binding globulin (SHBG), urinary estrogen metabolites and plasma F2-isoprostanes.

NCT ID: NCT00916877 Completed - Breast Cancer Clinical Trials

Prophylactic Cranial Irradiation in Patients With HER-2-Positive Metastatic Breast Cancer

Start date: November 2009
Phase: Phase 1
Study type: Interventional

Though brain metastases are a risk in all patients with breast cancer, those with HER-2 overexpression are at significantly greater risk. One series estimated a 30% incidence of brain metastases in this population, while another study found an incidence of approximately 40%. Traditional systemic therapies do not cross the blood brain barrier to any significant degree or at all, but radiation treatment can be effective in the treatment of intracranial metastases.

NCT ID: NCT00916825 Completed - Breast Cancer Clinical Trials

Impact of a Rehabilitation Programme for Mothers With Breast Cancer and Their Children

Start date: January 2009
Phase: N/A
Study type: Interventional

About 1/3 of newly diagnosed breast cancer patients are mothers of children who still live at home. They face additional challenges and stress, their children are also affected by the mother's illness. The oncological rehabilitation programme "getting better together" focuses on these special family needs. This waiting-control-group study examines the effectiveness of the intervention by accompanying the patients and their children over the course of a year and assessing their quality of life and psychological health.

NCT ID: NCT00916578 Completed - Breast Cancer Clinical Trials

Xeloda (Capecitabine) and External Beam Radiation

Start date: June 5, 2009
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to find out if Xeloda® (capecitabine) and radiation therapy can help to control breast cancer that did not respond well to chemotherapy. The safety of this study treatment will also be studied.

NCT ID: NCT00916162 Completed - Breast Cancer Clinical Trials

Drug Withdrawal in Women With Progressive Breast Cancer While on Aromatase Inhibitor Therapy

Start date: August 2006
Phase: N/A
Study type: Observational

The purpose of this research study is to study the effects of stopping aromatase inhibitory (AI) therapy on breast cancer progression. Aromatase inhibitors 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 been 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 with inhibit the breast cancer cells. An improvement or stabilization of breast cancer has been observed after stopping therapy with tamoxifen, a different anti-estrogen therapy, and has been reported in the literature after stopping AI therapy. This research study will be the first study to formally test the rate of disease improvement (response) or stabilization after stopping AI therapy.