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Breast Cancer clinical trials

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NCT ID: NCT00466830 Completed - Breast Cancer Clinical Trials

Psychological and Social Factors That May Increase the Risk of Developing Chronic Pain After Surgery in Women With Breast Cancer

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

RATIONALE: Certain psychological and social factors may increase the risk of developing chronic pain after surgery. Evaluating these factors over time in patients who have undergone surgery for breast cancer may help doctors plan treatment and improve patients' quality of life. PURPOSE: This clinical trial is studying the psychological and social factors that may increase the risk of developing chronic pain after surgery in women with breast cancer .

NCT ID: NCT00465725 Completed - Breast Cancer Clinical Trials

A Study Comparing Oral Picoplatin With Intravenous Picoplatin in Subjects With Solid Tumors

Start date: April 2007
Phase: Phase 1
Study type: Interventional

Picoplatin is a new platinum-based chemotherapy drug that has been studied in a variety of cancers. Phase 1 and 2 studies have demonstrated that picoplatin may be effective in patients whose cancer returns or does not improve after treatment with chemotherapy. In these studies, picoplatin was administered intravenously. A capsule containing picoplatin has been formulated. This study will investigate the activity of the oral capsule in humans. Participants with advanced solid tumors will be enrolled.

NCT ID: NCT00464646 Completed - Breast Cancer Clinical Trials

Therapy With Bevacizumab (BEV), Epirubicin, and Cyclophosphamide Followed by Docetaxel Plus Trastuzumab and BEV Given as Neoadjuvant or Adjuvant Therapy for Women With Locally Advanced HER2 Positive Invasive Breast Cancer

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

The main purpose is to learn if adding bevacizumab to standard chemotherapy and trastuzumab to treat HER2-positive breast cancer will affect heart function. This study will evaluate: - How bevacizumab, given with chemotherapy, and then bevacizumab given with trastuzumab after surgery, will affect breast tumors - Side effects from adding bevacizumab to chemotherapy and trastuzumab - Whether adding bevacizumab to chemotherapy and trastuzumab for breast cancer will affect the heart - If receiving bevacizumab will have any effect on how patients recover from surgery

NCT ID: NCT00464516 Completed - Breast Cancer Clinical Trials

Preoperative Estetrol in Breast Cancer

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

The study is designed as a single-center, randomized, double-blind, placebo-controlled study in pre- and postmenopausal women who will undergo surgery for breast cancer. Subjects will either receive estetrol or placebo during a 2 week treatment period. Several biological markers, such as a cellular growth marker and cell death markers, will be assessed in the tumor tissue and surrounding normal tissue before and after the treatment period. During the 2 week interval between diagnosis of breast cancer and surgical resection, no therapy for breast cancer is usually administered.

NCT ID: NCT00463489 Completed - Breast Cancer Clinical Trials

Lifestyle Intervention Study in Adjuvant Treatment of Early Breast Cancer

LISA
Start date: August 2007
Phase: N/A
Study type: Interventional

The primary objective of this trial is to evaluate the effect of the addition of a 2 year, centrally delivered individualized, telephone-based lifestyle intervention focusing on weight management to a mailed educational intervention on Disease Free Survival in post-menopausal women with early stage breast cancer (hormone receptor positive), BMI ≥24-<40 kg/m2, who are receiving standard letrozole adjuvant therapy.

NCT ID: NCT00462891 Completed - Breast Cancer Clinical Trials

A Mammography FastTrack Program in Increasing the Number of Women Undergoing Breast Cancer Screening

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

RATIONALE: Screening may help doctors find breast cancer cells early and plan better treatment for breast cancer. The Mammography FastTrack program may be effective in increasing the number of patients who undergo mammography. PURPOSE: This randomized clinical trial is studying the use of a Mammography FastTrack program to increase the number of women who undergo mammography.

NCT ID: NCT00462696 Completed - Breast Cancer Clinical Trials

MRI in Evaluating Early Response to Chemotherapy in Women Receiving Chemotherapy for Infiltrating Breast Cancer

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

RATIONALE: Diagnostic procedures, such as magnetic resonance imaging (MRI), may help in learning how well chemotherapy works to kill breast cancer cells and allow doctors to plan better treatment. Drugs used in chemotherapy, such as epirubicin and docetaxel, may stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This clinical trial is studying MRI in evaluating early response to chemotherapy in women receiving chemotherapy for infiltrating breast cancer.

NCT ID: NCT00462410 Completed - Breast Cancer Clinical Trials

Effect of Advertisements on Treatment Compliance in Women With Breast Cancer

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

RATIONALE: Measuring how advertising affects treatment compliance in women with breast cancer may help doctors plan the best treatment. PURPOSE: This clinical trial is studying how advertisements affect treatment compliance in women with breast cancer.

NCT ID: NCT00461253 Completed - Breast Cancer Clinical Trials

Case-Control-Study on the Breast Cancer Risk of Mirena® Compared With Copper IUDs

Start date: October 2006
Phase: Phase 4
Study type: Observational

The objective of this study is to determine the breast cancer risk of Mirena® users compared to copper intrauterine device (IUD) users in a community-based case-control study.

NCT ID: NCT00459771 Completed - Breast Cancer Clinical Trials

Evaluating the Effect of Candesartan vs Placebo in Prevention of Trastuzumab-associated Cardiotoxicity

Start date: June 2007
Phase: Phase 3
Study type: Interventional

Evaluating the effect of the angiotensin II-receptor (AT1) blocker candesartan vs placebo in prevention of trastuzumab-associated cardiotoxicity in patients with primary breast cancer treated with trastuzumab.