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Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

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NCT ID: NCT01699867 Completed - Breast Cancer Clinical Trials

Computed Optical Margin Assessment for Breast Cancer Surgery, Phase I (Part A)

Start date: December 2012
Phase: N/A
Study type: Observational

This multi-center, prospective, open label study analyzed specimens from fifty subjects at two study sites. Patients scheduled to undergo breast-conserving surgery were recruited in accordance with the inclusion and exclusion criteria. The study period per subject was the time it took to assess the ex vivo breast tissue sample using the study device. Image review was conducted after surgery and compared to the margin status findings in the post-operative pathology report.

NCT ID: NCT01698918 Completed - Clinical trials for Hormone Receptor Positive Breast Cancer

Open-label, Phase II, Study of Everolimus Plus Letrozole in Postmenopausal Women With ER+, HER2- Metastatic or Locally Advanced Breast Cancer

BOLERO-4
Start date: March 7, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study was to assess the efficacy and safety of first-line treatment with everolimus plus letrozole in postmenopausal women with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2 negative (HER2-) locally advanced or metastatic breast cancer. Moreover, the study also aimed to investigate the efficacy and safety of second line treatment with everolumus plus examestane in participants whose disease progressed during everolimus plus letrozole therapy.

NCT ID: NCT01698658 Completed - Breast Cancer Clinical Trials

Ultrasound Tomography Using SoftVue in Diagnosing Women With Breast Cancer

Start date: October 2012
Phase: N/A
Study type: Interventional

This clinical trial studies ultrasound tomography using SoftVue in diagnosing women with breast cancer. New diagnostic procedures, such as ultrasound tomography using SoftVue, may help find and diagnose breast cancer.

NCT ID: NCT01697345 Completed - Breast Cancer Clinical Trials

Breast Cancer, Aromatase Inhibitor Therapy, and Sexual Functioning: The Effects of Vaginal Testosterone Therapy

Start date: February 2013
Phase: Phase 0
Study type: Interventional

It is well documented that women who have breast cancer may experience a decrease in quality of life and sexual functioning due to side effects from adjuvant endocrine therapy, typically aromatase inhibitors (AIs). Women taking AIs are more likely to report unpleasant urogenital and vaginal symptoms due to the physiologic suppression of estradiol. This treatment can impair sexual functioning and cause a decreased sexual health quality of life. At the present time, there are no Food and Drug Administration (FDA) approved medications for the vulvovaginal or sexual side effects related to the use of AIs. The lack of treatment options is concerning because the number of women diagnosed with breast cancer continues to increase; their longevity, also, continues to increase with the use of newer adjuvant chemotherapies. Local health care practitioners have observed that the benefits of vaginal testosterone for sexual health in breast cancer survivors are similar to the benefits of vaginal estrogen in women without breast cancer. The purpose of this study is to evaluate the impact of using a daily compounded vaginal testosterone cream for 4 weeks (28 days) on breast cancer survivor's reported experience of vulvovaginal symptoms accompanying the use of AIs and their associated quality of life and sexual functioning.

NCT ID: NCT01695226 Completed - Breast Cancer Clinical Trials

Randomized Controlled Phase II Trial of Pre-operative Celecoxib Treatment in Breast Cancer

Start date: February 2004
Phase: Phase 2
Study type: Interventional

Cyclooxygenase-2 (COX-2) is frequently over-expressed in primary breast cancer. There is evidence that COX-2 inhibition exerts anti-tumor effects in breast cancer. To further determine the effect of COX-2 inhibition in primary breast cancer, we aimed at studying the changes in breast cancer tissues of patients treated with the selective COX-2 inhibitor celecoxib. In a single-centre double-blinded phase II study, breast cancer patients were randomised to receive either pre-operative celecoxib (400 mg) or placebo twice daily for two to three weeks. We collected fresh-frozen pre-surgical biopsies (before treatment) and surgical excision specimens (after treatment) to assess the tumor changes by use a cDNA microarray, which allows to study the genome-wide changes at the transcriptional level.

NCT ID: NCT01694225 Completed - Breast Cancer Clinical Trials

Adherence Rate of Monthly Bubble Package Among Patients Prescribed Adjuvant Endocrine Therapy in Breast Cancer Survivors

Start date: July 2012
Phase: N/A
Study type: Interventional

This study aims to establish the feasibility of using a monthly bubble package to improve compliance rates among women prescribed adjuvant endocrine therapy.

NCT ID: NCT01693549 Completed - Breast Cancer Clinical Trials

Study of Cabazitaxel in Patients With Metastatic Breast Cancer Previously Treated With Taxanes

Start date: September 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether cabazitaxel is effective in the treatment of metastatic breast cancer.

NCT ID: NCT01692210 Completed - Breast Cancer Clinical Trials

The Effect of Dexmedetomidine of the Immune System

Start date: September 2012
Phase: N/A
Study type: Observational

The goal of this research study is to learn about how dexmedetomidine (a standard of care sedative) affects your immune system (your defenses against cancer) by measuring your white blood cell levels before and after surgery.

NCT ID: NCT01690702 Completed - Breast Cancer Clinical Trials

Study of Nab-Paclitaxel in High Risk Early Breast Cancer

GAIN-2
Start date: September 2012
Phase: Phase 3
Study type: Interventional

two-armed trial to compare E-nP-C against tailored dtEC-dtD in patients with high risk early breast cancer

NCT ID: NCT01689610 Completed - Clinical trials for Metastatic Breast Cancer

Non-interventional Study With Nab-Paclitaxel (Abraxane®)

NABUCCO
Start date: April 2012
Phase:
Study type: Observational

The purpose of this non-interventional study is to collect data on the efficacy and safety of Nab-Paclitaxel in the routine application.