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Breast Cancer clinical trials

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NCT ID: NCT00210145 Completed - Breast Cancer Clinical Trials

Socio-aesthetic Intervention on Body Image and Quality of Life in Women With Breast Cancer.

ASE K SEIN
Start date: October 2003
Phase: N/A
Study type: Observational

The aim of this study is to evaluate the impact of a socio-aesthetic intervention on body image and quality of life in post-surgical patients with mastectomy or tumorectomy for breast cancer.Two groups of randomized subjects were constituted. Patients of the experimental group received 2 or 3 aesthetic care during the first post-surgical week, whereas those of the control group not. Body image, quality of life and diverse other personality variables were assessed at three different times: surgical operation day before, exit day before of hospitalization and three months afterwards. Our general hypothesis is that subjects who receive aesthetic care report levels significantly higher of corporal satisfaction and of quality of life at the end of the hospitalization and three months later than patients of the control group.

NCT ID: NCT00209092 Completed - Breast Cancer Clinical Trials

Randomized Phase II Trial Induction Therapy for Early Stage Breast Cancer

Start date: August 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out if the combination of docetaxel and capecitabine can shrink the size of breast tumors and preserve the breast.

NCT ID: NCT00208871 Completed - Breast Cancer Clinical Trials

An Evaluation of Stereoscopic Digital Mammography for Earlier Detection of Breast Cancer and Reduced Rate of Recall

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

The primary goal of this study is to compare, within a clinical screening setting, the performance of stereoscopic digital mammography with standard (non-stereo) digital mammography in the detection of abnormalities in the breast, including early breast cancer.

NCT ID: NCT00208273 Completed - Breast Cancer Clinical Trials

Concomitant and Sequential Radiohormonotherapy in Adjuvant Breast Cancer

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

This trial will compare grade 2 or greater late skin toxicities of concomitant letrozole-radiotherapy and radiotherapy followed by letrozole as adjuvant therapy for postmenopausal women with receptor (estrogen receptor [ER] and/or progesterone receptor [PgR]) positive tumors. Each drug will be prescribed for 5 years.

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: NCT00206505 Completed - Breast Cancer Clinical Trials

Neoadjuvant Taxotere

Start date: January 1999
Phase: Phase 2
Study type: Interventional

The purposes of this study are to better understand how Taxotere causes tumors to become smaller and to find out how effective Taxotere is in treating the type of breast cancer that you have.

NCT ID: NCT00206466 Completed - Breast Cancer Clinical Trials

Biologic Correlative Taxotere/AC

TAX/AC
Start date: April 2002
Phase: Phase 2
Study type: Interventional

We are asking you to take part in a research study of biomarkers (characteristics or traits of the genes inside cancer cells). We want to learn if these biomarkers could help us learn how well your breast cancer may respond (improve) to chemotherapy (drugs to treat cancer).

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: NCT00204880 Completed - Breast Cancer Clinical Trials

Aging and Cancer Effects (ACE) Study

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

Hypotheses: 1. Subjective self-reported data can be used to accurately reflect functioning across the 5 key domains. 2. Cancer and its various treatment modalities will exert detrimental effects on the 5 key domains in older adults with cancer. 3. Some aspect of baseline patient characteristic will be predictive of cancer-related outcomes.

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.