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Breast Cancer clinical trials

View clinical trials related to Breast Cancer.

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NCT ID: NCT00833963 Completed - Breast Cancer Clinical Trials

A Study of Pregnancy and Pregnancy Outcomes in Women With Breast Cancer Treated With Trastuzumab, Pertuzumab in Combination With Trastuzumab, or Ado-Trastuzumab Emtansine

MotHER
Start date: January 14, 2009
Phase:
Study type: Observational [Patient Registry]

The MotHER Pregnancy Registry is a United States (U.S.)-based, prospective, observational cohort study in women with breast cancer who have been or are being treated with a trastuzumab (herceptin)-containing regimen with or without pertuzumab (perjeta) or ado-trastuzumab emtansine (kadcyla) during pregnancy or within 7 months prior to conception (regardless of cancer stage at the time of trastuzumab, pertuzumab, or ado-trastuzumab emtansine exposure).

NCT ID: NCT00830635 Completed - Breast Cancer Clinical Trials

Multimedia Educational Program for Patients With Early-Stage Prostate Cancer or Breast Cancer

Start date: September 2008
Phase: N/A
Study type: Interventional

RATIONALE: A multimedia educational program may help patients with newly diagnosed prostate cancer and breast cancer reduce distress, make informed treatment decisions, and improve quality of life. PURPOSE: This randomized clinical trial is studying how well a multimedia educational program works in patients with early-stage prostate cancer or breast cancer.

NCT ID: NCT00830271 Completed - Clinical trials for Breast Cancer Surgery

Vicryl Plus and Monocryl Plus in Breast Surgery

Start date: December 2008
Phase: N/A
Study type: Interventional

This is a randomised pilot study comparing conventional sutures (Vicryl and Monocryl) with antiseptic coated equivalents (Vicryl plus andf Monocryl plus) in elective breast surgery.

NCT ID: NCT00829959 Completed - Breast Cancer Clinical Trials

Attitudes About Childbearing And Fertility With Inherited Breast And Ovarian Cancer Syndromes (HBOC)

Start date: February 2009
Phase: N/A
Study type: Observational

Objectives: - To evaluate the attitudes and opinions of women undergoing genetic counseling for hereditary breast and ovarian cancer syndrome, both before and after testing, in regards to pregnancy and fertility Hypothesis: -Factors that will increase the percentage of women endorsing prenatal diagnostic testing will include a personal history of breast or ovarian cancer, having had a mother or sister die of breast or ovarian cancer, and testing positive for a BRCA mutation.

NCT ID: NCT00828516 Completed - Breast Cancer Clinical Trials

Using Traditional Acupuncture in the Management of Cancer Treatment Related Lymphoedema

AMWELL-SL
Start date: April 2008
Phase: N/A
Study type: Interventional

RATIONALE: Acupuncture and moxibustion may improve well-being and quality of life in patients with lymphedema caused by breast cancer or head, neck, and throat cancer. PURPOSE: This clinical trial is studying how well acupuncture given together with moxibustion works in improving well-being and quality of life in patients with breast cancer or head, neck, and throat cancer who are undergoing standard treatment for lymphedema.

NCT ID: NCT00828074 Completed - Breast Cancer Clinical Trials

Sorafenib and Vinorelbine in Treating Women With Stage IV Breast Cancer

Start date: November 2008
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as vinorelbine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving sorafenib together with vinorelbine may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of sorafenib when given together with vinorelbine and to see how well they work in treating women with stage IV breast cancer.

NCT ID: NCT00826488 Completed - Breast Cancer Clinical Trials

A Comparison of Breast Tomosynthesis Mammography and Conventional Breast Imaging in the Characterization of Breast Masses

Start date: March 2009
Phase: Phase 0
Study type: Interventional

The purpose of this study is to compare conventional breast imaging and diagnostic work-up (2 dimensional imaging) to digital breast tomosynthesis (3 dimensional imaging) in the appearance of non-calcified breast masses. It is thought that non-calcified breast masses will be better visualized with the new 3D technology.

NCT ID: NCT00826397 Completed - Breast Cancer Clinical Trials

Acupuncture for Aromatase Inhibitor Induced Joint Pain

Start date: June 2005
Phase: N/A
Study type: Interventional

This is a randomized, controlled, pilot study to determine the safety and efficacy of acupuncture as an adjunct to pharmacological treatment compared to pharmacological intervention alone for the treatment of musculoskeletal pain related to aromatase inhibitors (AI) in postmenopausal breast cancer patients. Twenty participants (20 in each arm) will be enrolled at the Breast Oncology clinic at Columbia University Medical Center (CUMC). Patients in the treatment arm will receive acupuncture administered twice weekly for six weeks and will be allowed to take pain medication as necessary. The control patients will initially receive pain medication alone, then will cross-over to the acupuncture arm after six weeks. The investigators hypothesize that acupuncture will reduce AI induced joint symptoms. The study will enroll a total of 40 patients, half of whom will be randomized to one of the two arms to receive acupuncture plus pharmacological treatment (arm A) or pharmacological treatment alone (arm B). Joint pain will be assessed by the BPI-SF score at baseline and six weeks. All patients will have a baseline BPI worst pain item (#2) ≥3 points on a scale of 0-10.

NCT ID: NCT00826085 Completed - Breast Cancer Clinical Trials

Phase 1/2 Study of ThermoDox With Approved Hyperthermia in Treatment of Breast Cancer Recurrence at the Chest Wall

DIGNITY
Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This is a research study to evaluate the effects of ThermoDox in combination with therapeutic heating of the chest wall in the treatment of recurrent regional breast cancer. The purpose of this study is to evaluate the bioequivalence of ThermoDox and measure efficacy in recurrent chest wall patients.

NCT ID: NCT00824876 Completed - Breast Cancer Clinical Trials

Orthostatic Tolerance in Mamma Cancer Patients After Anaesthesia

Start date: January 2009
Phase: N/A
Study type: Observational

The investigators want to investigate the effect of anaesthesia, on the ability to maintain upright posture immediately after surgery in mamma cancer patients. The investigators hypothesis is, that a standard anaesthesia does not effect the ability to maintain upright posture right after surgery.