Clinical Trials Logo

Breast Cancer clinical trials

View clinical trials related to Breast Cancer.

Filter by:

NCT ID: NCT01004562 Completed - Breast Cancer Clinical Trials

Collecting Information From Patients Enrolled in the Breast Specialized Program of Research Excellence

Start date: August 2007
Phase: N/A
Study type: Observational

RATIONALE: Collecting and storing information from patients with cancer to study in the future may help doctors learn more about cancer. PURPOSE: This study is collecting information from patients enrolled in the Breast Specialized Program of Research Excellence.

NCT ID: NCT01004172 Completed - Breast Cancer Clinical Trials

Carboplatin and Bevacizumab for Progressive Breast Cancer Brain Metastases

Start date: November 2009
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to determine how well the combination of bevacizumab and carboplatin works in treating breast cancer that has spread to the brain. Bevacizumab is an antibody (a protein that attacks a foreign substance in the body) that is made in the laboratory. Bevacizumab works differently from the way chemotherapy drugs work. Usually chemotherapy drugs attack fast growing cancer cells in the body. Bevacizumab works to slow or stop the growth of cells in cancer tumors by decreasing the blood supply to the tumors. When the blood supply is decreased, the tumors don't get the oxygen and nutrients they need to grow. Carboplatin is in a class of drugs known as platinum-containing compounds and has been approved for use in the treatment of ovarian cancer. Information from other research studies suggests that the combination of bevacizumab with carboplatin may be effective in treating breast cancer.

NCT ID: NCT01004081 Completed - Breast Cancer Clinical Trials

Hormone Receptor Positive Metastatic Breast Cancer (HR+ mBC) BIIB021 Plus Aromasin Schedule Finding

Start date: November 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and tolerability of 2 dosing regimens of BIIB021 in combination with exemestane in women whose HR+ breast cancer had progressed following treatment with a nonsteroidal aromatase inhibitor (AI).

NCT ID: NCT01003951 Completed - Breast Cancer Clinical Trials

Acupuncture for the Treatment of Chronic Lymphedema

Start date: October 2009
Phase: Phase 2
Study type: Interventional

Lymphedema is an accumulation of lymphatic fluid in the tissues that causes swelling, most often in the arms and/or legs, and occasionally in other parts of the body. Lymphedema can occur when lymph vessels are damaged or lymph nodes are removed. Lymphedema can develop right after breast cancer treatment or weeks, months, or even years later. For many people, available treatments for lymphedema are not effective. Recent evidence suggests that acupuncture may help reduce the symptoms of lymphedema. The purpose of this study is to determine the effects of acupuncture on chronic lymphedema. This study will look further at whether acupuncture can reduce lymphedema and help us to understand immune changes that may be associated with improvements in lymphedema.

NCT ID: NCT01003158 Completed - Breast Cancer Clinical Trials

Study Assessing Safety and Tolerability of AZD8931 Alone or in Combination With Paclitaxel in Japanese Patients.

Start date: October 2009
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to determine if AZD8931 can be safely administered in Japanese patients alone and in combination with weekly paclitaxel. The study will be conducted in two parts: a monotherapy and a combination part, where safe doses of study treatment will be determined.

NCT ID: NCT01002014 Completed - Breast Cancer Clinical Trials

Nipple Sparing Mastectomy - Cosmetic Outcomes

Start date: January 21, 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to observe the cosmetic outcomes, patient satisfaction, and complications after skin sparing mastectomy with preservation of the nipple areolar complex.

NCT ID: NCT01001728 Completed - Breast Cancer Clinical Trials

SuPr Study (Supine Versus Prone Treatment Position in Breast Radiotherapy)

SuPr
Start date: November 2008
Phase: Phase 3
Study type: Interventional

A randomised, two-arm, non-blinded crossover study investigating the impact of treatment position (prone versus supine) upon reproducibility of tumour bed position in patients undergoing breast radiotherapy following excision of early breast cancer.

NCT ID: NCT01000662 Completed - Breast Cancer Clinical Trials

Study Comparing Whole Breast Radiotherapy With a Daily Versus a Weekly Tumor

Start date: March 2009
Phase: Phase 3
Study type: Interventional

All patients (with Stages 0-II breast cancer) will receive an accelerated three week regimen of prone whole breast radiotherapy. The study intends to test the hypothesis that a weekly boost to the tumor bed, delivered on Friday, before the weekend break, is as well tolerated as the daily boost during accelerated prone radiotherapy.

NCT ID: NCT00999596 Completed - Breast Cancer Clinical Trials

Image Evaluation of Philips Philips MammoDiagnost DR Full Field Digital Mammography System (FFDM)

Start date: April 2010
Phase: Phase 3
Study type: Observational

The purpose of this investigation, using hardcopy film, is to compare the accuracy of the Philips MammoDiagnost DR (FFDM device) and screen-film (SF) mammography in detection of breast cancer among women undergoing screening or diagnostic mammography. Per the new FDA Guidance document for FFDM, accuracy in comparison to Screen-film is no longer required.

NCT ID: NCT00996632 Completed - Breast Cancer Clinical Trials

The Use of a High-frequency Ultrasonic Knife in Breast Cancer Surgery

UKBC
Start date: September 2000
Phase: N/A
Study type: Interventional

Background: Lymphatic stasis and seroma formation are common complications of axillary lymphadenectomy in breast cancer surgery. The investigators aim is to test the hypothesis that the use of an ultrasonic knife for axillary dissection reduces the total amount and duration of persistent drainage and length of hospital stay. Method: The investigators have conducted a randomized trial on 94 patients (1 male, 93 females, mean age 64.7 years) who presented to the investigators unit with operable breast carcinoma. Patients in group A (38 cases) were operated on using exclusively the ultrasonic knife. Patients in group B (56 cases) were operated on using the conventional diathermy knife.