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Breast Neoplasms clinical trials

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NCT ID: NCT05130840 Recruiting - Breast Cancer Clinical Trials

Monitoring for Cancer Spread to the Central Nervous System (CNS) in People With Breast Cancer

Start date: July 13, 2022
Phase: N/A
Study type: Interventional

The researchers doing this study think that performing scans of the brain and testing cerebrospinal fluid (CSF) in people with HER2-positive breast cancer may be an effective way of identifying the early onset of CNS metastases (such as brain cancer). If the researchers can identify the early onset of CNS metastases, they can immediately treat that cancer and possibly prevent it from worsening. Currently, people with breast cancer don't usually have scans of the brain or CSF testing unless they are experiencing symptoms of CNS metastases.

NCT ID: NCT05130801 Recruiting - Breast Cancer Clinical Trials

A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During Surgery

Start date: November 19, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find out whether pre-operative mpMRI using additional MRI sequences may improve surgical outcomes by providing more accurate information about the extent and acidity of the tumor than standard MRI, and to see whether the use of the fluorescent imaging agent pHLIP ICG and NIRF imaging during surgery is a safe approach that may allow the surgeon to see the tumor and nearby tissues that contain cancer cells more clearly and remove them completely. During the Phase IIa part of this study, the safe dose of pHLIP ICG will be used that makes it easy for the surgeon to see the tumor and the nearby tissues and structures that may contain cancer cells. This study is the first to test pHLIP ICG in people, and the first to test the use of pHLIP ICG with mpMRI and NIRF imaging in surgery for breast cancer.

NCT ID: NCT05125432 Recruiting - Breast Cancer Clinical Trials

Genetic Predictors to Acupuncture Response for Arthralgia Induced by Aromatase Inhibitors in Patients With Breast Cancer

Start date: November 25, 2021
Phase: N/A
Study type: Interventional

Purpose:Acupuncture for arthralgia induced by aromatase inhibitors in patients with breast cancer associated with screening of SNPs.

NCT ID: NCT05122494 Recruiting - Breast Cancer Clinical Trials

A Phase Ⅲ Study of the Efficacy and Safety of Hemay022+Aromatase Inhibitor(AI) in Participants With ER+/HER2+ Advanced or Metastatic Breast Cancer

Fillful-03
Start date: January 19, 2022
Phase: Phase 3
Study type: Interventional

This is a Phase III, randomized, multicenter, 2-arm, open-label clinical trial designed to compare the safety and efficacy of Hemay022+Aromatase inhibitor(AI) with that of capecitabine + lapatinib in participants with ER+/HER2+ locally advanced or metastatic breast cancer. Participants will be treated until disease progression (PD), unmanageable toxicity, or study termination. Once disease progression is reported, all participants will be followed for survival every 3 months until death, loss to follow-up.

NCT ID: NCT05120180 Recruiting - Clinical trials for Breast Cancer Lymphedema

Effect of ALND With Vein Branches Reservation on Postoperative Upper Limb Edema and Dysfunction in Breast Cancer

PLEDGE
Start date: January 3, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of axillary lymph node dissection with or without axillary vein branches reservation on the affected upper limb edema and dysfunction in breast cancer patients, and to explore the solutions to prevent the affected upper limb edema and dysfunction after ALND.

NCT ID: NCT05116449 Recruiting - Clinical trials for Breast Cancer Female

Comparison of Changes in the Quality of Life of Patients Operated on Breast Cancer at the Drôme Ardèche Breast Institute According to Access to Supportive Oncological Care (IDSein)

IDSein
Start date: February 22, 2021
Phase:
Study type: Observational

The aim of this study is to explore the quality of life of cancer patients, in particular women operated on breast cancer, throughout their care journey, taking into account their access to supportive oncological care within and outside the establishment care.

NCT ID: NCT05115474 Recruiting - Clinical trials for Triple Negative Breast Cancer

Study of Screening Brain MRIs in Stage IV Breast Cancer

Start date: December 21, 2021
Phase:
Study type: Observational

The study is a single arm, nonrandomized phase II prospective study, with the goal of investigating the role of screening brain MRIs in neurologically asymptomatic patients with metastatic breast cancer.

NCT ID: NCT05114720 Recruiting - Breast Cancer Clinical Trials

Moxifloxacin in Adjuvant Treatment of Patients With Operable Breast Cancer

Start date: November 11, 2021
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to compare disease-free survival (DFS) of patients with operable breast cancer randomised to treatment with standard adjuvant chemotherapy plus moxifloxacin or placebo.

NCT ID: NCT05113485 Recruiting - Breast Cancer Clinical Trials

UCLA Breast Cancer Survivor Health Promotion Research Study

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

Pilot randomized controlled parallel group behavior change comparative effectiveness trial involves 30 breast cancer survivors interested in losing excess body fat. Both interventions include dietary + exercise prescriptions that hold promise for reducing the survivors' risk of cancer recurrence. Both interventions are consistent with the Dietary Guidelines for Americans but the Diabetes Prevention Program (DPP)-based approach focuses on weight loss through calorie restriction and increased physical activity while the Highly Microbiota-Accessible Foods (HMAFs) approach is intended to be a low-numeracy version of a Mediterranean-style diet and increased physical activity. The DPP approach is considered to be a high-numeracy intervention because it requires that consumers keep track of all calories consumed and expended per day and to endeavor to maintain a calorie deficit each day during the active weight loss phase. For both conditions, the 12 to 13-week intervention includes 2 virtual home visits, 2 virtual group education sessions and 7 telephone or Zoom-based coaching sessions by well-trained intervenors. Assessments occur at baseline and six months, with systemic inflammation (high sensitivity C-reactive protein) being the primary outcome measure and visceral fat being a secondary outcome. Other prespecified secondary outcomes include gut microbiota alpha-1 diversity, insulin resistance, HDL-cholesterol, daily count of highly microbiota-accessible foods, waist circumference, BMI, systolic blood pressure, ratio of fecal Proteobacteria to short chain fatty acid-generating bacteria and health-related quality of life.

NCT ID: NCT05112341 Recruiting - Clinical trials for Study on Breast Cancer Patients

Adjuvant Whole Breast Irradiation in Five Fractions Versus Fifteen Fractions in Early Breast Cancer

Start date: June 1, 2021
Phase:
Study type: Observational

the study aiming for compairing results of hypofractionaton radiotherapy treatment in patient with early breast cancer between two arms the first arm recieving five fractions and the other arm recieving fifteen fraction