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Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

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NCT ID: NCT00196859 Completed - Breast Cancer Clinical Trials

Study in Elderly Patients With Early Breast Cancer (ICE)

Start date: June 2004
Phase: Phase 3
Study type: Interventional

This trial is done to determine the role of adjuvant chemotherapy with capecitabine in patients ≥ 65.

NCT ID: NCT00196846 Completed - Breast Cancer Clinical Trials

Prevention of Chemotherapy Induced Ovarian Failure With Goserelin in BC Patients (ZORO)

Start date: March 2005
Phase: Phase 2
Study type: Interventional

Study done in young breast cancer patients to prevent chemotherapy induced ovarian failure

NCT ID: NCT00196820 Completed - Breast Cancer Clinical Trials

Mono Efficacy of Capecitabine (MoniCa)

Start date: July 2005
Phase: Phase 2
Study type: Interventional

Study done in patients with metastatic breast cancer in order to determine the efficacy of capecitabine

NCT ID: NCT00195026 Completed - Breast Cancer Clinical Trials

Infrared Imaging (Breast Scan IR) for Early Breast Cancer Detection

Start date: March 2005
Phase: N/A
Study type: Observational

This protocol will evaluate a new non-invasive infrared imaging system as an adjunctive tool for breast cancer detection that has been approved by the FDA. The technology and device have been developed by Infrared Sciences Corp. and has undergone more than 3 years of testing prior. The subject device's utility will be investigated with regard to its sensitivity toward breast cancer, however it records temperature data and other physiological parameters of the breast, and compares them to a database of patients with known breast health.

NCT ID: NCT00195013 Completed - Breast Cancer Clinical Trials

Randomized Placebo-Controlled Trial of Glutamine for Breast Cancer Patients With Peripheral Neuropathy

Start date: December 2003
Phase: Phase 3
Study type: Interventional

Patients with breast cancer receiving paclitaxel chemotherapy who have mild symptoms of peripheral neuropathy will receive glutamine or placebo to try and improve symptoms.

NCT ID: NCT00194779 Completed - Clinical trials for HER2-positive Breast Cancer

Combination Chemotherapy and Filgrastim Before Surgery in Treating Patients With HER2-Positive Breast Cancer That Can Be Removed By Surgery

Start date: October 2003
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well giving combination chemotherapy and filgrastim together before surgery works in treating patients with human epidermal growth receptor 2 (HER2)-positive breast cancer that can be removed by surgery. Drugs used in chemotherapy, such as doxorubicin hydrochloride, cyclophosphamide, and paclitaxel work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving combination chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Colony-stimulating factors, such as filgrastim, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of chemotherapy. Giving doxorubicin hydrochloride, cyclophosphamide, and filgrastim together followed by paclitaxel before surgery may be an effective treatment for breast cancer

NCT ID: NCT00194766 Completed - Breast Cancer Clinical Trials

Continuous Temozolomide in Patients With Advanced or Metastatic Soft Tissue Sarcoma or Metastatic Breast Cancer

Start date: July 2000
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether treatment with temozolomide can effect the survival of patients with advanced breast cancer or soft tissue sarcoma.

NCT ID: NCT00194753 Completed - Breast Neoplasm Clinical Trials

Adjuvant Therapy for High-Risk Breast Cancer With Wkly Adriamycin & Oral Cytoxan With G-CSF for 12 Wks; Wkly Taxol x 12

Start date: December 2001
Phase: Phase 2
Study type: Interventional

The primary objectives of the study are to evaluate the feasibility and toxicity of treatment with 12 weeks of Adriamycin with daily oral Cytoxan with G-CSF support followed by 12 weeks of Taxol. Feasibility will be assessed by comparing the delivered dose intensity of each drug to the delivered dose intensity in previous trials. Toxicity will be assessed by comparing the incidence and severity of toxicity with these drugs to previous trials using these drugs in the same combination. We hypothesize metronomic, dose dense treatment as given in this study will be less toxic and more effective than historical regimens using the same drugs in a less metronomic, dose dense manner.

NCT ID: NCT00194740 Completed - Breast Neoplasm Clinical Trials

Taxotere Plus Weekly Navelbine and G-CSF: A Study in Stage IV Breast Cancer

Start date: November 1997
Phase: Phase 2
Study type: Interventional

The two drugs used to treat metastatic breast cancer in this study may perform better when used together than when used separately. The use of another drug that prevents the most common side effect of the two-drug combination permits the delivery of both agents at closer to the "full" dose for either when used alone. We hypothesize that the two-drug combination used with G-CSF support will be more effective and less toxic than other standard regimens for the treatment of metastatic breast cancer.

NCT ID: NCT00194727 Completed - Breast Neoplasm Clinical Trials

Weekly Vinorelbine and Oral Capecitabine as Treatment for Stage IV Breast Cancer

Start date: May 2002
Phase: Phase 2
Study type: Interventional

The primary purpose of the study is to examine the safety and effectiveness of combination therapy consisting of daily oral capecitabine and weekly intravenous vinorelbine in stage IV breast cancer subjects. The study is designed to assess the safety and effectiveness of this combination therapy. Safety will be assessed by analyzing the types of toxicity, the severity of toxicity and the need for dose modification or delay due to toxicity. Effectiveness will be assessed by analyzing response rates, time to treatment failure, time to progression and overall survival. Our hypothesis is that the regimen will be more effective than standard historic regimens for this type and stage of cancer.