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Breast Cancer clinical trials

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NCT ID: NCT02103946 Withdrawn - Breast Cancer Clinical Trials

Serratus Anterior Plane Block Versus Paravertebral Block for Postmastectomy Analgesia

SAM
Start date: April 2014
Phase: N/A
Study type: Interventional

ًًًُُُُThe investigators are testing the efficacy of a new novel technique; serratus anterior plane block, for preventing postoperative pain after breast surgery for cancer. This block will be compared with the well-established paravertebral block.

NCT ID: NCT02102438 Withdrawn - Breast Cancer Clinical Trials

Chemotherapy for Elderly Patients Diagnosed With Localized HER2 Positive Breast Cancer

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

There is major concern regarding chemotherapy related toxicity in the group of women older than 65 years old diagnosed with human epidermal growth factor receptor 2 (HER2) positive breast cancer (BC). Nevertheless, these patients are at a particularly high risk of breast cancer recurrence and death. Of note, older patients may experience higher risk for Trastuzumabe related cardiotoxicity, especially when this agent is combined with an anthracycline. Recent studies have shown extremely favourable outcomes in early HER2+ BC patients treated with a combination of paclitaxel and trastuzumab, omitting anthracyclines from treatment. Investigators sought to investigate safety and outcome data on a cohort of elderly patients treated with weekly paclitaxel combined with carboplatin and trastuzumab.

NCT ID: NCT02079272 Withdrawn - Breast Cancer Clinical Trials

REBECCA Study (RadiothErapy for BrEast Cancer and CArdiotoxicity)

REBECCA
Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a new technique of radiotherapy for breast cancer (helical tomotherapy) can induce cardiac toxicity that would be detected in the first two years after treatment. Screening of subclinical cardiac lesions with non-invasive cardiac imaging techniques combined with measures of circulating biomarkers of cardiac tissue lesions and coronary lesions would allow assessing radiation-induced cardiac toxicity at an early stage.

NCT ID: NCT02067637 Withdrawn - Breast Cancer Clinical Trials

Delayed Effects of Treatment in Cancer Survivors (DETECS)

DETECS
Start date: March 2014
Phase: N/A
Study type: Observational

Hypotheses and Specific Aims: There is limited data on the long-term consequences of cancer therapy on young, reproductively aged cancer survivors. The investigators objective is to characterize some of these effects in the cancer population.

NCT ID: NCT02067416 Withdrawn - Breast Cancer Clinical Trials

PREDATOR: Neoadjuvant Gene Prediction for Breast Cancer

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

Study of the assay, Mammostrat®. to verify its utility as a predictor or outcome tool to determine whom would benefit from chemotherapy prior to surgery. Also could be used as a clinical marker to identify patients with breast cancer who do not benefit from some preoperative chemotherapies.

NCT ID: NCT02058667 Withdrawn - Breast Cancer Clinical Trials

Reirradiation With Concurrent Paclitaxel for Breast Cancer

Start date: July 2014
Phase: Phase 1
Study type: Interventional

The purpose of this trial in addition to a dose finding study for concurrent Paclitaxel, will be to establish a treatment algorithm for chest wall reirradiation. A nominal margin of at least 5cm will be used on the protocol and extending it to 7cm. Considering the standard treatment of breast cancer incorporates a cumulative dose of 60Gy, delivering an additional 50.4 Gy followed by a boost should target a total dose of 120 Gy.

NCT ID: NCT02053597 Withdrawn - Breast Cancer Clinical Trials

TRIal evalUating the Menstrual and Ovarian Function of Young Breast Cancer Patients Treated With a cycloPHosphamide-free Regimen

TRIUMPH
Start date: October 2014
Phase: Phase 2
Study type: Interventional

Recently, there has been a rising trend of delaying childbearing and hence more women are diagnosed with breast cancer before completing their families. Given the continuous decline in recurrences and death secondary to breast cancer and the reassuring data on the safety of pregnancy following breast cancer more women are inquiring into the possibility of preserving fertility following chemotherapy. The challenge remains in using a regimen that is devoid of cyclophosphamide, but is as effective as the standard regimens that incorporate cyclophosphamide. The combination doxorubicin (50 mg/m2) and paclitaxel (200 mg/m2) (AP) followed by 12 weeks of paclitaxel (80 mg/m2) (P) emerges as a treatment option with convincing results regarding its effectiveness in the early setting, and could be potentially associated with less ovarian toxicity being devoid of cyclophosphamide.

NCT ID: NCT02035085 Withdrawn - Breast Cancer Clinical Trials

19F Hot Spot MRI of Human Adipose-derived Stem Cells for Breast Reconstruction

CS-1000
Start date: June 2014
Phase: Phase 1
Study type: Interventional

Six female patients (>18 years of age, pre-menopausal) who have had loco-regional (lumpectomy and radiation) therapy for breast carcinoma and have been at least one-year disease free will undergo liposuction, the autologous SVF cell fraction will be isolated and labeled with CS-1000 in the operating room without entering cell culture, which will then be returned to the patient at the site of breast grafting. Patients will receive a pre-screening MRI . Patients will have an MRI scans over a period of 1 month at Johns Hopkins. Follow-up MRIs at 6,12, and 18 months will also be performed. Only at Johns Hopkins with fluorine being done as part of this investigational study. By performing fluorine MRI and quantification of 19F signal, we hypothesize that the engraftment of transplanted cells can be tracked in ways not possible before, using the total fluorine signal as surrogate marker for cell persistence and survival. We expect that a clinically successful outcome (maintenance of breast contour and volume) will be positively correlated with cell survival. The outcome of this study may pave the way for using 19F MRI cell tracking as a new tool for stem cell therapy in a variety of clinical applications.

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: NCT01959867 Withdrawn - Breast Cancer Clinical Trials

SurgiMend in Two-stage Implant-based Breast Reconstruction in Patients With Pre-Mastectomy Radiotherapy

Start date: January 2017
Phase: N/A
Study type: Interventional

This is a prospective clinical study comparing two-stage breast reconstruction following mastectomy with and without the use of SurgiMend® PRS fetal bovine collagen matrix in patients with pre-mastectomy radiation therapy.