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Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

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NCT ID: NCT03538171 Active, not recruiting - Clinical trials for Advanced Breast Cancer

Ph3 Study of Exemestane With or Without Entinostat in Chinese Patients With Hormone Receptor-Positive, Locally Advanced or Metastatic Breast Cancer

Start date: May 15, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this randomized phase III trial is to evaluate the clinical benefit of combining entinostat with exemestane in Chinese patients with HR-positive, HER2-negative, locally advanced or metastatic breast cancer, who have disease progression on endocrine therapy. Additionally,the safety, tolerability, and PK profile of the treatment combination are evaluated.

NCT ID: NCT03536897 Recruiting - Breast Cancer Clinical Trials

IORT Following Breast Conserving Surgery for Early Stage Breast Cancer Registry

Start date: February 27, 2018
Phase:
Study type: Observational [Patient Registry]

This is a prospective, registry trial which will enroll women aged 65 and above with early stage, low risk breast cancer who will be treated with partial mastectomy and intraoperative radiation therapy (IORT). The primary aim is to determine the 5-year risk of in-breast tumor recurrence. Secondary aims include identification of acute- and late-toxicity, cosmetic result, disease-free survival and overall survival.

NCT ID: NCT03535961 Completed - Breast Cancer Clinical Trials

Apatinib Combined With Oral Etoposide in Metastatic HER2 Negative Breast Cancer

Start date: May 1, 2017
Phase: Phase 2
Study type: Interventional

The hypothesis of this study is to discover if the all-oral therapy with apatinib plus oral Etoposide can shrink or slow the growth of pretreated HER2 negative metastatic breast cancer.

NCT ID: NCT03535701 Completed - Clinical trials for Stage IV Breast Cancer AJCC v6 and v7

Ketogenic Diet and Chemotherapy in Affecting Recurrence in Patients With Stage IV Breast Cancer

KETO-CARE
Start date: October 20, 2017
Phase: N/A
Study type: Interventional

This pilot clinical trial studies how well a ketogenic diet and chemotherapy work in affecting the return of cancer in patients with stage IV breast cancer. Ketogenic diet may be more effective than standard nutrition and may affect quality of life, inflammation, and tumor-related changes. Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving ketogenic diet and chemotherapy may be better in patients with breast cancer.

NCT ID: NCT03534570 Recruiting - Heart Diseases Clinical Trials

Gated Radiotherapy in Left Sided Breast Cancer Patients

GATTUM
Start date: May 2018
Phase:
Study type: Observational

To assess the need of respiratory gated radiotherapy in left sided breast cancer patients.

NCT ID: NCT03532087 Withdrawn - Breast Neoplasms Clinical Trials

Study to Identify the Impact of Denosumab on the Immune System in Patients With HER2 Negative Breast Cancer

PERIDENO
Start date: February 2018
Phase: Phase 2
Study type: Interventional

The aim of this prospective, randomized, multicenter, open-label, explorative phase II study is to identify the impact of (neo)adjuvant denosumab on the systemic immunity and local immunologic microenvironment in postmenopausal patients with HER2 negative non-metastatic primary breast cancer.

NCT ID: NCT03530722 Completed - Breast Cancer Clinical Trials

Ex-vivo Performance Evaluation of the Histolog™ Scanner for Human Breast Carcinoma Detection on Fresh Breast Core Biopsies

Start date: July 4, 2017
Phase:
Study type: Observational

Fresh breast core biopsies suspicious for breast cancer that are usually taken during clinical breast assessments will be imaged via confocal microscopy. The device so called HistologTM Scanner is based on confocal fluorescence and displays microscopic histology images superficial layers of fresh tissue. After the imaging procedure the fresh breast tissue specimen will be followed according to the gold standard workflow (H&E-stained images). Subsequently, two pathologists will analyze the HistologTM Scanner obtained-images and H&E-stained images for potential breast cancer structures. A comparison of both analyses for cancer visualization will be performed to evaluate the feasibility of using confocal microscopy for breast cancer detection.

NCT ID: NCT03530696 Completed - Breast Cancer Clinical Trials

T-DM1 and Palbociclib for Metastatic HER2 Breast Cancer

T-DM1
Start date: December 6, 2018
Phase: Phase 2
Study type: Interventional

This is a single arm, phase II study to evaluate if the combination of T-DM1 with palbociclib improves progression-free survival in patients with metastatic HER2 positive breast cancer. All patients will be treated with T-DM1 with palbociclib.

NCT ID: NCT03529565 Active, not recruiting - Bone Pain Clinical Trials

Histamine and Bone Pain Association in Participants With Breast Cancer Metastatic in the Bone

Start date: January 31, 2019
Phase:
Study type: Observational

This trial studies histamine and bone pain association in participants with breast cancer that has spread to the bone. Studying histamine levels in samples of blood from participants with breast cancer in the laboratory may help doctors learn more about reducing cancer bone pain and preventing further bone metastasis.

NCT ID: NCT03529383 Completed - Breast Cancer Clinical Trials

Efficacy of Exercise Using Connected Activity Trackers and Therapeutic Education in Localized Breast Cancer

DISCO
Start date: May 18, 2018
Phase: N/A
Study type: Interventional

The 3-year DISCO study aims to systematically implement physical activity in breast cancer patients. The primary objective is to investigate the efficacy of a connected device (personalized non-supervised exercise program including a wristband as activity tracker, a smartphone application, and a website) and the efficacy of a therapeutic education program on the physical activity level of patients at the end of the 6-month programs. The research hypothesis is that patients participating in the intervention with the connected device or in the therapeutic education program will achieve the international recommendations in terms of physical activity, compared to women receiving only physical activity recommendations.