Clinical Trials Logo

Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

Filter by:

NCT ID: NCT00207324 Completed - Breast Neoplasms Clinical Trials

The Use of Silver Leaf Dressing in the Prevention of Radiotherapy Induced Skin Reactions

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

The hypothesis is that silver leaf nylon dressing reduces the percentage of patients developing brisk erythema and moist desquamation while undergoing whole breast radiotherapy. The secondary hypothesis is that silver leaf nylon dressing reduces breast-related symptoms of pain, itching and burning sensation in patients receiving whole breast radiotherapy.

NCT ID: NCT00206518 Completed - Breast Cancer Clinical Trials

Taxotere and Adriamycin/Cytoxan (AC) Validation in Breast Cancer Patients

TACAC
Start date: September 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to learn if the biomarker information obtained (learned or received) from the earlier studies can tell us whether or not Taxotere and/or Adriamycin/Cytoxan can cause tumors to become smaller.

NCT ID: NCT00206492 Terminated - Breast Cancer Clinical Trials

Trial of ZD1839 (Iressa) and Tamoxifen in Breast Cancer Patients

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

The researchers want to learn whether ZD1839 can improve the activity of tamoxifen, a drug that participants will receive for the treatment of the type of breast cancer being studied. Tamoxifen medicine is part of the standard treatment for the type of breast cancer being studied. It is approved for the treatment of this problem. In order to help the researchers understand how the cancer responds to these medicines, the researchers will take a small tissue sample (biopsy) of the breast cancer before beginning treatment and after two weeks of treatment, at 6 weeks and when surgery is done as part of treatment for the cancer. If participants do not respond to treatment, another biopsy will be done to see why the participants did not respond. These samples will also be collected to look at different characteristics of the cancer. The researchers cannot and do not guarantee that participants will benefit if they take part in this study

NCT ID: NCT00206453 Terminated - Breast Cancer Clinical Trials

Extension Neoadjuvant Taxotere: Study of the Effects of Taxotere in Patients With Breast Cancer

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

We, the investigators at Baylor Breast Care Cancer, are doing this study to learn how well Taxotere makes tumors become smaller. We are also doing this study to find out how well Taxotere treats the type of breast cancer that some patients have. We are asking patients to take part in this study because they have locally advanced breast cancer. Women with this breast cancer will usually receive chemotherapy medicines to reduce or shrink the cancer before surgery to take out the cancer. If patients choose to take part in this study, they will receive Taxotere and the combination of cyclophosphamide and doxorubicin. These medicines are part of the standard good medical care for this type of breast cancer. They are approved for the treatment of this problem. To help us learn how the patients' cancer responds to these medicines, we will take a small tissue sample (biopsy) of the patients' breast cancer before beginning treatment, one day after the first dose of treatment, once each week for the first three weeks of treatment, and when surgery is done as part of treatment for their cancer. These samples will be collected also to look at the biology of the patients' cancer. We will also use a new method called cDNA array technology, which lets us look at thousands of genes (coding information inside the cancer cell) at once. By looking at different genes in the breast cancer, we may learn important information about which cancers will respond to a chemotherapy medicine. We hope to learn if there are different gene patterns in patients whose tumors shrink or do not shrink with this chemotherapy medicine. This information may help us, in the future, to choose the right medicines for women with breast cancer so that they have the highest chance of their cancer shrinking with chemotherapy medicine. We cannot and do not know if patients will benefit if they take part in this study.

NCT ID: NCT00206427 Completed - Breast Cancer Clinical Trials

Neoadjuvant GW572016 to Treat Breast Cancer

GW
Start date: August 2004
Phase: Phase 2
Study type: Interventional

We want to learn whether GW572016 is effective in breast cancers that have HER2.

NCT ID: NCT00206414 Terminated - BREAST CANCER Clinical Trials

Arimidex/Faslodex/Iressa Study: A Trial Using Arimidex, Faslodex and Iressa in Women With Breast Cancer

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

The investigators want to know if combining Arimidex and Faslodex with Iressa will be an effective treatment for breast cancer. They also want to know, using special tests on the tumor, the changes that occur with the treatment so they can try to improve their treatment for breast cancer in the future.

NCT ID: NCT00204776 Completed - Clinical trials for Metastatic Breast Cancer

XELOX for Metastatic Breast Cancer

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

Both capecitabine and oxaliplatin have single agent activity in breast cancer. The combination has improved activity in other solid tumors. This study seeks to assess the activity of the combination in breast cancer.

NCT ID: NCT00204490 Completed - Breast Cancer Clinical Trials

Soy Isoflavones and Breast Cancer Risk Reduction

Start date: April 2004
Phase: Phase 2
Study type: Interventional

Soy consumption has been associated with reduced risk for developing breast cancer. Soy contains isoflavones which are weak estrogens. The roles of soy isoflavones in reducing breast cancer risk are currently unclear. Breast density has been considered as a breast cancer risk marker. We hypothesize that because isoflavones have estrogen-like activities, breast density and possibly bone density will be lower in women on soy-isoflavones.

NCT ID: NCT00204477 Completed - Breast Cancer Clinical Trials

Soy Protein and Breast Cancer Risk Reduction

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

Soy consumption has been associated with reduced risk for developing breast cancer. Ovarian hormones and breast density are considered breast cancer risk markers. We propose to test the hypothesis that consumption of soy protein reduces ovarian steroid hormones and results in a corresponding reduction in breast density comparing to casein protein.

NCT ID: NCT00203502 Completed - Breast Cancer Clinical Trials

Primary Systemic Therapy in Operable/Locally Advanced Breast Cancer

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

The main purpose of this study is to find out what effects taking the drug bevacizumab together with two chemotherapeutic agents, docetaxel and cyclophosphamide followed by doxorubicin alone before surgery will on breast cancer. Bevacizumab will be given for twelve weeks in combination with chemotherapy then it ill be held during the administration of doxorubicin. Twenty-eight to fifty-six days after undergoing surgery, all patients will receive nine three-weekly infusions of bevacizumab.