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Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

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NCT ID: NCT01383174 Completed - Breast Neoplasms Clinical Trials

Nuevo Amanecer: Promoting the Psychosocial Health of Latinas

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether a new program Nuevo Amanecer (A New Dawn), improves the quality of life of Latinas diagnosed with breast cancer. Trained Latina counselors who have had breast cancer provide support to recently diagnosed women. The investigators call these counselors peer support counselors.

NCT ID: NCT01382082 Enrolling by invitation - Breast Cancer Clinical Trials

Assessment of Cognitive Function in Breast Cancer and Lymphoma Patients Receiving Chemotherapy

CANTAB
Start date: July 14, 2011
Phase:
Study type: Observational

Cognitive impairments in cancer patients represent an important clinical problem. Studies to date estimating prevalence of difficulties in memory, executive function, and attention deficits have been limited by small sample sizes and many have lacked healthy control groups. More information is needed on promising biomarkers and allelic variants that may help to determine the etiology of impairment, identify those most vulnerable to impairment, and develop interventions for these difficulties. This is a longitudinal observational study of cognitive function in breast cancer and lymphoma patients receiving chemotherapy to better understand the prevalence of cognitive difficulties (i.e., problems with memory, executive function, and attention) in these populations.

NCT ID: NCT01381874 Completed - Postmenopausal Clinical Trials

A Study of Abiraterone Acetate Plus Prednisone With or Without Exemestane in Postmenopausal Women With Estrogen Receptor-Positive (ER+) Metastatic Breast Cancer Progressing After Letrozole or Anastrozole Therapy

Start date: August 24, 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of oral abiraterone acetate plus oral prednisone and oral abiraterone acetate plus oral prednisone plus oral exemestane, each compared with oral exemestane alone, in postmenopausal women with estrogen receptor-positive (ER+) metastatic (spreading) breast cancer that has relapsed after treatment with letrozole or anastrozole.

NCT ID: NCT01380925 Completed - Breast Cancer Clinical Trials

The Jewels in Our Genes Study - an African American Family Study of Breast Cancer

Start date: October 2010
Phase: N/A
Study type: Observational

The research team is studying why some African American families have multiple cases of breast cancer. This study will help to better understand if there are undiscovered genes unique to African Americans that may predict early breast cancer risk. Breast cancer survivors AND their relatives who are also breast cancer survivors are being recruited to the study.

NCT ID: NCT01380912 Recruiting - Breast Cancer Clinical Trials

Can Methylprednisoloneacetate Prevent Seroma After Mastectomy for Primary Breast Cancer

Start date: August 2010
Phase: N/A
Study type: Observational

A randomised double-blinded study, in which the patients either get methylprednisoloneacetate or saline solution in the mastectomy cavity to evaluate the efficacy of methylprednisoloneacetate in preventing seroma in patients operated for primary breast cancer.

NCT ID: NCT01380808 Completed - Clinical trials for Metastatic Breast Cancer

Capecitabine and Pseudomonas Aeruginosa Combination in Metastatic Breast Cancer (MBC)

Start date: May 2011
Phase: Phase 2
Study type: Interventional

The progression free survival could be prolonged adding pseudomonas aeruginosa to monotherapy capecitabine.

NCT ID: NCT01380353 Completed - Breast Cancer Clinical Trials

Test Uniformity of Transdermal Drug Delivery to Breast Using Diclofenac Epolamine

Start date: June 2011
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to look for ways to improve breast cancer treatment by giving breast cancer drugs through the skin of the breast. The drug used in this study is a diclofenac epolamine patch and is a nonsteroid anti-inflammatory pain reliever. The drug amount that gathers in the breast, after application of a patch to the skin of the breast, will be measured and compared to the amount that is found in the breast when the patch is applied to the skin of the belly.

NCT ID: NCT01378533 Recruiting - Breast Cancer Clinical Trials

The Trial Comparing Dose-dense AC-T With PC as Adjuvant Therapy for TNBC

Start date: May 2011
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to compare the 3 years DFS of dose-dense epirubicin and cyclophosphamide followed by paclitaxel with paclitaxel plus carboplatin as adjuvant therapy for triple-negative breast cancer. The other purpose of this trial is to observe the patient's tolerance.

NCT ID: NCT01377363 Completed - Breast Cancer Clinical Trials

Evaluation of Degree of Conversion of HER2 Receptor Between Primary Breast Cancer and Metastasis

Start date: December 11, 2009
Phase:
Study type: Observational

This is a Prospective Clinical Trial without drugs, to determine the HER2 status in the metastasis of patients with primary breast cancer HER2. 32 Sites have been taking part in this Clinical Trial.

NCT ID: NCT01377324 Completed - Clinical trials for Metastatic Breast Cancer

Molecular Imaging of Fulvestrant Effects on Availability of ER Binding Sites

Start date: May 2011
Phase: Phase 2
Study type: Interventional

The dose of fulvestrant to optimally downregulate estrogen receptors (ER) is currently subject of debate. Effects of fulvestrant on the ERs may be evaluable by molecular imaging using positron emission tomography with the ER-specific FES tracer. In this pilot study we will evaluate the effects of the new dose of fulvestrant (500mg i.m.)on the availability of ER binding sites in 15 metastatic breast cancer patients.