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Breast Neoplasms clinical trials

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NCT ID: NCT03615573 Active, not recruiting - Breast Cancer Clinical Trials

Survey Study: Financial Impact of Breast Cancer Treatment

Start date: September 4, 2018
Phase:
Study type: Observational

A survey study to evaluate the financial impact of breast cancer as self-reported by breast cancer patients over a period of 1 year. The study will also look at the health insurance literacy and patient's utilization of support services.

NCT ID: NCT03615430 Completed - Breast Cancer Clinical Trials

Serratus Plane Block in Preventing Postoperative Pain of Mastectomy

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

A prospective, double-blinded randomized controlled, 1-year follow-up study was designed to compare the analgesic effect of serratus plane block (SPB) after breast cancer surgery. Women undergoing radical mastectomy were dIvided into Control group and SPB group. The postoperative acute pain was evaluated by numerical rating scale (NRS) and the effect of preventing chronic pain was assessed at 3, 6, 12 months after surgery by NRS.

NCT ID: NCT03613220 Completed - Clinical trials for HR+ HER2 Breast Cancer

CompLEEment-1 Canadian Correlative Sub-Study

LEEomic
Start date: December 28, 2018
Phase: Phase 2
Study type: Interventional

Collection of tumor and blood samples from subjects enrolled in the main study (LEE011A2404) will undergo proteomic and ctDNA analysis respectively to better understand mechanisms of response and resistance to ribociclib in combination with letrozole therapy.

NCT ID: NCT03613181 Not yet recruiting - Brain Metastases Clinical Trials

ANG1005 in Leptomeningeal Disease From Breast Cancer

ANGLeD
Start date: December 2023
Phase: Phase 3
Study type: Interventional

This is an open-label Phase 3 study to see if ANG1005 can prolong survival compared to a Physician Best Choice control in HER2-negative breast cancer patients with newly diagnosed leptomeningeal disease and previously treated brain metastases.

NCT ID: NCT03612934 Completed - Breast Cancer Clinical Trials

The Impact of SPC on Advanced Breast Cancer Patients

Start date: May 1, 2015
Phase:
Study type: Observational

The aim of this prospective, observational study is the evaluation of the effectiveness of a 14-day Specialist Palliative Care therapy in participants with advanced breast cancer carried out in a stationary palliative care unit in Poland. The length of the entire study will be 36 months.

NCT ID: NCT03612648 Active, not recruiting - Breast Cancer Clinical Trials

Three Fraction Accelerated Partial Breast Irradiation as the Sole Method of Radiation Therapy for Low-risk Stage 0 and I Breast Carcinoma

Start date: August 30, 2018
Phase: N/A
Study type: Interventional

The investigators proposed approach allows them to deliver a low total dose of radiation to patients with low-risk, early-stage breast cancer which would further minimize the impact of adjuvant therapy. This work has the potential to revolutionize partial breast irradiation by allowing it to take place at many radiation oncology centers with minimal specialized equipment beyond that commonly available. The investigators first step is this proposed single institution phase I/II study designed primarily to evaluate the tolerance of this approach which the investigators are choosing to call Three Fraction APBI (Tri-APBI).

NCT ID: NCT03612596 Completed - Breast Cancer Clinical Trials

Narrative Visualization for Breast Cancer Survivors' Physical Activity

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

This study tests the feasibility and acceptability of a physical activity intervention that combines use of a wearable activity monitor with a scrapbook. Half of the participants will receive this enhanced intervention, while the other half will receive a wearable activity monitor with a standard step log.

NCT ID: NCT03611985 Withdrawn - Breast Cancer Clinical Trials

Phase I/IIa Study of Pharmacokinetics and Safety of Epidiferphane™ and Taxanes in Breast Cancer Patients

Start date: March 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Patients with breast cancer are commonly treated with taxane chemotherapy. Some very common side effects of taxanes, such as anemia and peripheral neuropathy, are often as not well addressed during treatment, resulting in dose reductions, dose delays and early discontinuation (collectively called relative dose intensity) of these chemotherapy agents in 15-80 % of patients on these drugs. This reduction in relative dose intensity (RDI) results in worse clinical outcomes such as progression free and overall survival. Pre-clinical studies in mouse models subjected to standardized chemotherapy regimens containing paclitaxel or oxaliplatin have shown that the nutritional supplement Epidiferphane™ reduces both neuropathy and anemia. This study will investigate whether the use of Epidiferphane™ in patients with breast cancer receiving taxane chemotherapy results in an attenuation of the side effects experienced, as well as an improvement in tumor response rate. The safety and maximum tolerated dose of Epidiferphane™ in this patient population will also be determined in this study.

NCT ID: NCT03611543 Completed - Breast Cancer Clinical Trials

Evaluating Image Quality and Comfort of an Investigational Curved Paddle Compared to a Standard Paddle

Start date: October 20, 2016
Phase:
Study type: Observational

The goal of this study is to evaluate patient comfort during compression with a standard flat mammographic paddle and an investigational curved paddle. This is a study that will be performed with x-ray imaging and will be used to determine if an overall reduction in pain can be appreciated in patients without loss in image quality as compared to the current standard mammogram. Another benefit of the curved paddle may be an increase of perceivable and measurable tissue capture.

NCT ID: NCT03609671 Completed - Breast Cancer Clinical Trials

Emotions Immunology and Breast Cancer

Start date: November 23, 2015
Phase: N/A
Study type: Interventional

Pilot study representing a proof of concept regarding the potential for immune system enhancement with psychotherapy, resulting in improved immunological response at lumpectomy or mastectomy in patients undergoing neoadjuvant chemotherapy.