Clinical Trials Logo

Breast Cancer clinical trials

View clinical trials related to Breast Cancer.

Filter by:

NCT ID: NCT00234195 Completed - Breast Cancer Clinical Trials

Wellbutrin XL, Major Depressive Disorder and Breast Cancer

Start date: September 2005
Phase: Phase 4
Study type: Interventional

- To evaluate the efficacy of bupropion extended release (Wellbutrin XL™) in the treatment of Major Depressive Disorder in women with breast cancer. - To evaluate the tolerability of bupropion extended-release (Wellbutrin XL™) in these patients

NCT ID: NCT00233974 Completed - Breast Cancer Clinical Trials

Molecular Marker Profiling of Axillary Lymph Nodes in Predicting Response in Patients With Locally Advanced or Metastatic Breast Cancer Who Are Undergoing Chemotherapy Followed By Surgery

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

RATIONALE: Comparing results of diagnostic procedures, such as molecular marker profiling, done before and after chemotherapy, may help doctors predict a patient's response to treatment and help plan the best treatment. PURPOSE: This phase II trial is studying how well molecular marker profiling of axillary lymph nodes works in predicting response in patients with locally advanced or metastatic breast cancer who are undergoing chemotherapy followed by surgery.

NCT ID: NCT00232661 Completed - Breast Cancer Clinical Trials

PROACT - Pre-Operative Arimidex Compared To Tamoxifen

Start date: August 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare tamoxifen, versus a newer treatment, ARIMIDEX, which we already know to be well tolerated. The main objectives of this research study are to see whether using these drugs will shrink down tumours before surgery and to see if any shrinkage in the tumour affects the extent of surgery that is required.

NCT ID: NCT00232505 Completed - Breast Cancer Clinical Trials

Cetuximab + / - Carboplatin for Estrogen Receptor-Negative, Progesterone Receptor-Negative Metastatic Breast Cancer

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

RATIONALE: Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Cetuximab may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. It is not yet known whether giving cetuximab together with carboplatin is more effective than giving cetuximab alone in treating metastatic breast cancer. PURPOSE: This randomized phase II trial is studying cetuximab and carboplatin to see how well they work compared with cetuximab alone in treating women with estrogen receptor-negative (ER-), progesterone receptor-negative (PR-) metastatic breast cancer.

NCT ID: NCT00232479 Completed - Breast Cancer Clinical Trials

Dose Dense Carboplatin, Taxotere and Herceptin As Primary Systemic Therapy in Breast Cancer

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

Dose dense therapy has been shown to increase survival in the adjuvant setting of breast cancer. It is unknown if dose dense therapy will improve survival in tumors that express her-2. This study evaluates a neoadjuvant regimen containing carboplatin, taxotere and herceptin when used in a dose dense manner in patients with large breast cancers. The endpoint of pathologic complete response is used as a surrogate marker for survival.

NCT ID: NCT00230711 Completed - Breast Cancer Clinical Trials

Physical Activity Promotion in Cancer Follow-Up Care

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

This study aims at testing the efficacy of a physical activity (PA)intervention in an outpatient oncology setting. We plan to compare Brief Advice for PA (MD advice plus contact control) vs. Extended Advice (MD advice plus telephone-based PA counseling by research staff) over 3 months among 300 women who have completed treatment for breast cancer in the past 2 years. Specific Aims: The primary aim is to examine the effects of oncologists' advice on PA plus telephone counseling (Extended Advice) vs. oncologists' advice (Brief Advice) alone on minutes of moderate-intensity PA at 3 months among 300 sedentary women who have completed treatment for breast cancer. Secondary aims include examining a) the effects of the two interventions on participants' moderate-intensity PA at 6 and 12 months, b) the effects of the interventions on participants' physical functioning, fatigue, vigor and quality of life (QOL) at 3, 6 and 12 months, and c) the acceptability of the interventions to the oncologists and the usefulness of the interventions to patients.

NCT ID: NCT00228943 Completed - Breast Cancer Clinical Trials

The Role of Serotonin in Hot Flashes After Breast Cancer

Start date: July 2005
Phase: N/A
Study type: Interventional

The purpose of this proposal is to improve our understanding of the role of tryptophan and serotonin in hot flashes. The main hypothesis is that alterations in tryptophan and serotonin levels are involved in the induction of hot flashes in women with breast cancer and genetic variations in the serotonin receptors and transporters also play a role.

NCT ID: NCT00228930 Completed - Breast Cancer Clinical Trials

Tamoxifen Pharmacogenetics and Clinical Effects

Start date: September 2002
Phase: Phase 4
Study type: Observational

The purpose of this research is to try to identify which women who take tamoxifen are likely to suffer from hot flashes or are more likely to have other side effects or benefits from the drug. The researchers will do so by determining whether there are mutations that normally occur in human DNA that might influence the way individuals respond to medications.

NCT ID: NCT00226967 Completed - Breast Cancer Clinical Trials

Stress, Diurnal Cortisol, and Breast Cancer Survival

Start date: September 8, 2002
Phase:
Study type: Observational

The purpose of this study is to learn about the effects of stress on hormones, the relationship between these hormones and cancer progression.

NCT ID: NCT00225927 Completed - Clinical trials for Breast Cancer Invasive Nos

Trial Comparing Radioactive Seed Localization to Standard Procedure for Non-palpable Breast Cancers

Start date: June 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a new surgical technique (radioguided seed localization) for localizing nonpalpable breast tumours is better than the standard technique (needle localization).