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Breast Neoplasms clinical trials

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NCT ID: NCT01975597 Terminated - Clinical trials for Metastatic Breast Cancer

Pilot Study of Bone Biopsy and Aspirate in Women With Metastatic Breast Cancer

Start date: August 2013
Phase:
Study type: Observational

This is a feasibility study to demonstrate the team's ability to collect bone marrow aspirates and biopsies for research purposes from women with metastatic breast cancer.

NCT ID: NCT01975363 Completed - Clinical trials for Ductal Breast Carcinoma in Situ

Pilot Study of Curcumin for Women With Obesity and High Risk for Breast Cancer

Start date: June 2013
Phase: N/A
Study type: Interventional

This randomized pilot clinical trial studies a nanoemulsion formulation of curcumin in reducing inflammatory changes in breast tissue in obese women at high risk for breast cancer. Curcumin may reduce inflammation in breast tissue and fat. This may affect the risk of developing breast cancer.

NCT ID: NCT01975142 Completed - Clinical trials for Metastatic Breast Cancer, HER2 Negative Primary Tumor

Validity of HER2-amplified Circulating Tumor Cells to Select Metastatic Breast Cancer Considered HER2-negative for Trastuzumab-emtansine (T-DM1) Treatment.

Start date: November 7, 2013
Phase: Phase 2
Study type: Interventional

Patients with metastatic breast cancer considered HER2 negative are screened for HER2-amplified circulating tumor cells. If at least HER2-amplified circulating tumor cell is detected, patients are treated by Trastuzumab - Emtansine (T-DM1) in a single arm phase II with an adaptive design.

NCT ID: NCT01975064 Completed - Breast Neoplasms Clinical Trials

Cancer and Anesthesia: Survival After Radical Surgery - a Comparison Between Propofol or Sevoflurane Anesthesia

CAN
Start date: November 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether anesthesia maintained with propofol results in better one- and five-year-survival than anesthesia maintained with sevoflurane.

NCT ID: NCT01973660 Completed - Breast Cancer Clinical Trials

PAM50 HER2-enriched Phenotype as a Predictor of Response to Dual HER2 Blockade in HER2-positive Early Breast Cancer

PAMELA
Start date: October 2013
Phase: Phase 2
Study type: Interventional

Non-randomized, open label, multicentric translational research study in women with untreated invasive breast carcinoma eligible for primary surgery (Stage I-IIIA). The aim of PAMELA is to test the hypothesis that PAM50 HER2-enriched (HER2-E) subtype better predicts response to neoadjuvant dual anti-HER2 blockade, with or without endocrine therapy, compared to traditional clinical HER2 classification. Furthermore, we posit that characterization of gene expression patterns may identify profiles of those who may be safely spared chemotherapy.

NCT ID: NCT01973309 Completed - Clinical trials for Metastatic Breast Cancer

A Study of Vantictumab (OMP-18R5) in Combination With Paclitaxel in Locally Recurrent or Metastatic Breast Cancer

Start date: September 2013
Phase: Phase 1
Study type: Interventional

This is an open-label Phase 1b dose-escalation study to assess the safety, tolerability, and PK of vantictumab when combined with paclitaxel.

NCT ID: NCT01972984 Completed - Breast Cancer Clinical Trials

Feasibility Study of Presurgical Hormone Therapy (Anastrozole) in Breast Cancer Patients

NEO ER 11-05
Start date: October 2012
Phase: Phase 2
Study type: Interventional

1. Women with operable breast cancer with a 2-8 week preoperative waiting period will accept preoperative therapy trials and specifically taking a standard drug for breast cancer such as anastrozole in this study 2. Short term anastrozole treatment will induce measurable changes in biomarker levels (ER, PR, Her2, Ki67) within the tumor. 3. Degree of response to short term anastrozole varies with a) duration of treatment and b) breast cancer subtype (based on initial pre-treatment biomarker status)

NCT ID: NCT01972048 Withdrawn - Breast Cancer Clinical Trials

Mobile Phone Multimedia Messaging Intervention for Breast Cancer Screening

Start date: January 2014
Phase: N/A
Study type: Interventional

Korean American (KA) women have among the highest breast cancer mortality rates and lowest breast cancer screening rates of U.S. American women across racial/ethical groups. This innovative project seeks to harness mobile phone technology as a means to take preventative health care to a new level among this population. Using the Fogg Behavioral Model this study proposes to develop a mobile phone-based intervention designed to motivate KA women to undergo an annual mammogram (mMammogram). The overall study aim is to develop and assess the feasibility and effectiveness of a 7-day long mMammogram intervention designed to persuade KA women to undergo breast cancer screening.

NCT ID: NCT01969643 Completed - Clinical trials for Triple Negative Breast Neoplasms

A Safety Study of SGN-LIV1A in Breast Cancer Patients

Start date: October 22, 2013
Phase: Phase 1
Study type: Interventional

This study will examine the safety and tolerability of ladiratuzumab vedotin (LV) in patients with metastatic breast cancer. LV will be given alone or in combination with trastuzumab.

NCT ID: NCT01969253 Completed - Breast Cancer Clinical Trials

A Prospective Observational Study of Lymphedema in Breast Cancer With Axillary Lymph Node Dissection

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

Over the past few years, several studies have been made on various outcomes about the incidence of lymphedema. Because the outcomes can be came out differently each study by measurement, criteria, treatment period, treatment method and morbid extremities of lymphedema. Therefore it is required for understanding about the incidence, risk factor and physical progress for to be treated and prevented of lymphedema. Also it is necessary that to understand characteristics of lymphedema measurements and to establish diagnostic criteria of lymphedema through comparative study. The aim of this study was to analyze the incidence and risk factor of lymphedema through prospectively observation, and to determine effects on the quality of life of lymphedema after breast cancer surgery with ALND.