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Breast Cancer clinical trials

View clinical trials related to Breast Cancer.

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NCT ID: NCT03383679 Completed - Clinical trials for Breast Cancer Female

Study on Androgen Receptor and Triple Negative Breast Cancer

START
Start date: March 14, 2018
Phase: Phase 2
Study type: Interventional

This is a multicenter uncontrolled, open-label, prospective, non-comparative randomized, phase II study. Patients will be randomized between darolutamide in Arm n°1 (two-stage Simon's design) and capecitabine in Arm n°2 with two patients randomized in Arm n°1 for one patient randomized in Arm n°2. The trial population is composed of women over 18 years old with triple-negative and androgen receptor positive, locally recurrent (unresectable) or metastatic breast cancer.

NCT ID: NCT03383107 Completed - Breast Cancer Clinical Trials

Effect of Radiotherapy Variables on Circulating Effectors of Immune Response and Local Microbiome

Start date: January 22, 2018
Phase:
Study type: Observational

Exposure to radiation can impact immune cells that are present in the blood, such as lymphocytes. It is hypothesized that larger radiation fields and/or longer courses of radiation, result in greater decrease in immune cells. To test this hypothesis, investigators will take blood samples from subjects undergoing two different standard of care radiation regimens for prostate cancer, and subjects undergoing two different standard of care regimens for breast cancer.

NCT ID: NCT03381417 Completed - Clinical trials for Breast Cancer Female

Nanogen Pegcyte Clinical Study for the Prevention of CIN in Breast-cancer Patients.

Start date: October 6, 2016
Phase: Phase 3
Study type: Interventional

Accelerated AC regimen-Doxorubicin 60 mg/m2,Cyclophosphamide 600 mg/m2 on day 1 & day 14 of each cycle along with G-CSF support for up to 4 cycles, followed by Paclitaxel 175 mg/m2 in the next 4 cycles is the standard clinical practice in Vietnam for breast cancer, this regimen is to facilitate the dose-dense schedule, patients receive every-2-week therapy along with G-CSF support. the accelerated dose-dense schedule improve disease-free and overall survival among women with breast cancer .Primary objective of this study is to compare the efficacy and safety of Nanogen's Pegcyte and Roche's Neulastim for prevention of chemotherapy (Accelerated AC regimen)-induced neutropenia on breast cancer patients. Breast cancer patients scheduled to receive myelosuppressive chemotherapy (AC regimen) will be recruited in this trial. All eligible patients receive single subcutaneous injection of study drugs 24 hours after chemotherapy administration in each cycle for 3 consecutive cycles. Efficacy and safety assessments will be assessed based on the incidence of severe neutropenia in combination of temperature > 38.3℃ or sepsis or life threatening infection and incidence of serious adverse events.

NCT ID: NCT03377816 Completed - Pain Clinical Trials

The Role of Emotional Processing in Improving the Quality of Life of Breast Cancer Patients

REPAT
Start date: June 11, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to examine two mechanistic changes: emotion processing (awareness, expression and acceptance) and cholinergic anti-inflammatory processes (HRV and cytokine expression) through which an Art Therapy (AT) intervention reduces depression, pain and fatigue.

NCT ID: NCT03376503 Completed - Breast Cancer Clinical Trials

Nanogen Pegfilgrastim (Pegcyte) PK/PD Clinical Study in Breast Cancer Patients

Start date: May 25, 2016
Phase: Phase 1
Study type: Interventional

Breast cancer patients scheduled to receive myelosuppressive chemotherapy (AC regimen) will be enrolled in this study. Eligible patients receive single SC injection of pegcyte or neulastim 24 hours after administration of chemotherapy (Doxorubicin and Cyclophosphamide) in the first cycle (14 days each cycle). Blood samples are collected to determine the serum concentration of investigational drugs at specific time points in the first cycle. Absolute neutrophil count, CD34+ count, Cmax (maximum serum concentration), AUC0-t (area under the curve of the plasma concentration time) and Tmax (time required to reach Cmax) will be calculated from the serum concentration profile

NCT ID: NCT03375892 Completed - Breast Cancer Clinical Trials

The Use of Deep Inspiration Breath Hold and Prone Irradiation to Decrease Cardiac Radiation Exposure

Start date: March 3, 2018
Phase: N/A
Study type: Interventional

This study aims to discover more about radiation techniques for people treated for left-sided breast cancer that minimizes exposure to the heart, as noted by mean heart dose.

NCT ID: NCT03375827 Completed - Breast Cancer Clinical Trials

Feasibility of an Individualized Goals of Care Discussion Guide for Advanced Breast Cancer

Start date: January 22, 2018
Phase: N/A
Study type: Interventional

This research study is evaluating whether asking patients to fill out a brief survey about their goals and preferences for care and giving this survey to their clinician before the next visit helps improve communication and decision-making in breast cancer care.

NCT ID: NCT03375801 Completed - Breast Cancer Clinical Trials

Implementing a Decision Aid for Breast Cancer and DCIS Patients Deciding on Their Radiation Treatment.

BRASA
Start date: October 1, 2017
Phase: N/A
Study type: Interventional

This is a pre-and post intervention study on the effect and implementation of an personalized decision aid for woman with breast cancer who face a decision on their radiation treatment.

NCT ID: NCT03374995 Completed - Breast Carcinoma Clinical Trials

Topical Keratin in Treating Radiation Dermatitis in Patients With Breast Cancer

Start date: March 26, 2018
Phase: N/A
Study type: Interventional

This randomized pilot clinical trial studies how well topical keratin works in treating radiation dermatitis in patients with breast cancer. Radiation dermatitis is a skin condition that is a common side effect of radiation therapy. The affected skin becomes painful, red, itchy, and blistered. Topical keratin may help to improve skin appearance and hydration in patients with breast cancer.

NCT ID: NCT03373474 Completed - Clinical trials for Breast Cancer Lymphedema

Warm Acupuncture for Breast Cancer Related Lymphedema

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

The purpose of this study is to clarify whether local-distal point association is more effective than local point association by warm acupuncture in the management of breast cancer related lymphedema.