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Breast Cancer clinical trials

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NCT ID: NCT00291122 Completed - Breast Cancer Clinical Trials

An Examination of Predictors of Indicators of Response to Celecoxib in Women Who Have a Diagnosis of Early Breast Cancer

Start date: January 2003
Phase: Phase 1
Study type: Observational

To assess the quantitative real time PCR results results of oligonucleotide probes for a number of gene transcription products that may be useful as predictors of indicators of response to celecoxib.

NCT ID: NCT00291109 Completed - Breast Cancer Clinical Trials

An Examination of Predictors of Indicators of Response to Letrozole 2.5 mg

Start date: January 2003
Phase: Phase 1/Phase 2
Study type: Observational

To assess the quantitative real time PCR results of oligonucleotide probes for a number of gene transcription products that may be useful as predictors or indicators of response to letrozole

NCT ID: NCT00291083 Completed - Breast Cancer Clinical Trials

Protocol for Postmenopausal Women at Increased Risk of Developing Breast Cancer

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

To examine nipple aspirate fluid for secretions that may be identified as a high risk indicator for development of breast cancer, and compare those to serum analysis.

NCT ID: NCT00290745 Completed - Breast Cancer Clinical Trials

Tamoxifen or Letrozole in Treating Women With Ductal Carcinoma in Situ

Start date: February 19, 2002
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Estrogen can cause the growth of breast cancer cells. Hormone therapy using tamoxifen or letrozole may fight breast cancer by blocking the use of estrogen by the tumor cells or by lowering the amount of estrogen the body makes. PURPOSE: This clinical trial is studying how well tamoxifen or letrozole work in treating women with ductal carcinoma in situ.

NCT ID: NCT00290732 Completed - Breast Cancer Clinical Trials

Liposomal Doxorubicin Before Mastectomy in Treating Women With Invasive Breast Cancer

Start date: November 2005
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as liposomal doxorubicin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving chemotherapy in different ways, such as into the breast ducts, may kill more tumor cells. Giving chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This phase I trial is studying the side effects and best dose of liposomal doxorubicin when given before mastectomy in treating women with invasive breast cancer.

NCT ID: NCT00289432 Completed - Breast Cancer Clinical Trials

Hospital Based Group Intervention for Breast Cancer Patients.

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

INCAM-study is a multicenter, prospective, randomized controlled trial. The aim of the study is to test the effectiveness of psychoeducative intervention when offered in hospital setting as a component of routine breast cancer care. The hypotheses are; - that breast cancer patients participating in psychoeducative interventions focusing on coping will experience better health-related quality of life than those who participate in the hospital standardised psychoeducative intervention. - that coping styles are associated with the immune system.

NCT ID: NCT00288249 Completed - Breast Neoplasms Clinical Trials

Safety and Efficacy Study of a New Chemotherapy Agent to Treat Metastatic Breast Cancer

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

The purpose of this study is to determine whether the study drug is effective and safe in the treatment of patients with metastatic breast cancer

NCT ID: NCT00288002 Completed - Breast Cancer Clinical Trials

Combination Chemotherapy With or Without Capecitabine and/or Trastuzumab Before Surgery in Treating Women With Stage I, Stage II, or Stage III Breast Cancer

Start date: January 2005
Phase: Phase 3
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as epirubicin, cyclophosphamide, docetaxel, and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways. Some find tumor cells and kill them or carry tumor-killing substances to them. Others interfere with the ability of tumor cells to grow and spread. Giving combination chemotherapy together with monoclonal antibodies before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving monoclonal antibodies after surgery may kill any tumor cells that remain after surgery. It is not yet known whether combination chemotherapy is more effective with or without capecitabine and/or trastuzumab in treating breast cancer. PURPOSE: This randomized phase III trial is studying epirubicin, cyclophosphamide, and docetaxel to compare how well they work with or without capecitabine and/or trastuzumab before surgery in treating women with stage I, stage II, or stage III breast cancer.

NCT ID: NCT00287898 Completed - Breast Cancer Clinical Trials

Telephone-Based Genetic Counseling or Standard Genetic Counseling in Women at Risk of Carrying the BRCA1 or BRCA2 Mutation

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

RATIONALE: Genetic counseling may work as well over the telephone as it does in-person. It is not yet known whether genetic counseling by telephone is more effective than standard (in-person) genetic counseling in women at risk of carrying the BRCA1 or BRCA2 mutation. PURPOSE: This randomized phase III trial is studying telephone-based genetic counseling to see how well it works compared to standard (in-person) genetic counseling in women at risk of carrying the BRCA1 or BRCA2 mutation.

NCT ID: NCT00287534 Completed - Breast Cancer Clinical Trials

Effectiveness of Combination of Arimidex and Nolvadex in Adjuvant Therapy of Breast Carcinoma in Postmenopausal Women.

ARNO-95
Start date: November 1996
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy and tolerability of 3 years treatment with anastrozole after a prior 2 years' treatment with tamoxifen versus 5 years treatment with tamoxifen in postmenopausal women with early breast cancer