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Breast Neoplasms clinical trials

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NCT ID: NCT04496492 Completed - Breast Cancer Clinical Trials

Preoperative Use of Tocotrienol From Annatto Bixa Orellana L. in Breast Cancer Patients: a Prospective Clinical Trial.

TOCANNATO
Start date: February 9, 2016
Phase: Phase 2
Study type: Interventional

Tocotrienols have shown strong in vitro and in vivo anti-oxidant and anticancer activity, promoting apoptosis and regulating oncogenic targets in breast cancer. However their clinical use is still experimental especially in preoperative setting, where there are still no data of antioxidant and antiinflammatory beneficial roles. This study is a prospective observational clinical study enrolling 50 patients with primary breast cancer (T1-2, N0-1, M0) who received 4-weeks oral treatment of delta-T3 before surgery (200 mg/twice daily) with personalized nutritional and psychoeducational support. This study evaluates the effects of treatment on oxidant (tock fast-Li Starfish) and antioxidant capacity (TAC Track, Li Starfish), anti-inflammatory activity (complete profiling of adaptive and innate cell immunity, immunologic serum markers (miRNA)), immunological response on tumor (gene expression profiling on preoperative tissue tumor biopsy and on surgical specimen), TNF-alpha, IL-6 and VEGF and proliferation/apoptosis, anti-inflammatory and anti-oxidant activity of breast cancer cell lines. This study evaluates the effects of treatment on oxidant (tock fast-Li Starfish) and antioxidant capacity (TAC Track, Li Starfish), on anti-inflammatory activity (complete profiling of adaptive and innate cell immunity, immunologic serum markers (miRNA)), on immunological response on tumor (gene expression profiling on preoperative tissue tumor biopsy and on surgical specimen), on TNF-alpha, IL-6 and VEGF, on proliferation/apoptosis, anti-inflammatory and anti-oxidant activity of breast cancer cell lines.

NCT ID: NCT04494958 Completed - Clinical trials for Triple Negative Breast Cancer

Palbociclib and Binimetinib in Advanced Triple Negative Breast Cancer

PALBOBIN
Start date: November 18, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

This study is an interventional, prospective, multicentric, single-arm, open label, phase Ib clinical trial. This study will be carried out in patients diagnosed of metastatic or locally advanced unresectable triple negative breast cancer with activation of ERK and/or CDK4/6 in which the following will be assesed: the overall response rate, the aggregation of antitumor effect depending on the different kinome profiles and the safety profile to the combination of palbociclib and binimetinib.

NCT ID: NCT04487561 Completed - Breast Cancer Clinical Trials

Hemopatch Versus Axillary Drainage After Axillary Lymphadenectomy

REDHEMOPACH
Start date: March 1, 2020
Phase: N/A
Study type: Interventional

Aspirative drainage continues to be the "gold standard" for the management of this post-surgical complication, even though it can lead to complications such as obstruction of the drainage, peritubal leakage of the seroma, etc. This may result in pain and reduction in mobility of the affected arm. Based on our positive clinical outcomes and the fact that there is not any published data available in the literature regarding this use of the patch, the investigators propose a multicentric, randomized controlled clinical trial, with the objective of comparing the Hemopatch® with the usual technique used (aspirative drainage) in terms of efficacy and safety. Hypothesis: Placing a Hemopatch ® instead of an aspirative drainage in women after undergoing axillary lymph node dissection during breast cancer surgery may reduce the appearance of seroma and consequently the need for a puncture, as well as the complications related to aspirative drainage.

NCT ID: NCT04483505 Completed - Clinical trials for Breast Cancer Metastatic

Rogaratinib, Palbociclib y Fulvestrant in Patients With Breast Cancer.

ROGABREAST
Start date: November 25, 2020
Phase: Phase 1
Study type: Interventional

This study is an open, multicenter, prospective phase I dose escalation clinical trial followed by an expansion cohort. The aim of this study is to asses the Recommended Phase 2 Dose (R2PD) and the safety profile, among other efficacy, in FGFR1/2/3 positive, hormone receptor-positive breast cancer (HRPBC) patients with metastatic disease after progression to the combination of an aromatase inhibitor plus palbociclib, abemaciclib or ribociclib, according RECIST 1.1 criteria.

NCT ID: NCT04482803 Completed - Clinical trials for Location and Biopsy of Axillary Lymph Nodes

Targeted Biopsy of Carbon Nanoparticles Labelled Axillary Node for cN+ Breast Cancer

Start date: September 24, 2020
Phase: N/A
Study type: Interventional

To explore the feasibility of target biopsy of carbon nanoparticles labelled lymph node after neoadjuvant systemic therapy for cN+ breast cancer, and evaluate whether it can accurately predict axillary lymph node status after neoadjuvant systemic therapy.

NCT ID: NCT04480437 Completed - Breast Cancer Clinical Trials

Multi-parametric Breast Ultrasound Imaging as a Potential Biomarker for Breast Cancer

mp-BUS
Start date: November 15, 2020
Phase: N/A
Study type: Interventional

It is studied whether multi-parametric biomarkers such as speed-of-sound imaging or others, applied during breast ultrasound (BUS) imaging allows to classify lesions according to its malignancy. The standard reference intervention is BUS guided biopsy or the consensus of the board of experts judging the BUS imaging results if no biopsy is done.

NCT ID: NCT04480229 Completed - Clinical trials for Breast Cancer Female

Telenursing and Breast Cancer: The Turkish Case

Start date: May 6, 2016
Phase: N/A
Study type: Interventional

This study aims to determine the effectiveness of telenursing services on chemotherapy symptoms and comfort levels in patients with breast cancer in Turkey.

NCT ID: NCT04479098 Completed - Clinical trials for Breast Neoplasm Female

Effects of Training and Detraining on Postmenopausal Breast Cancer Survivors

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

The present study aimed to verify the effects of resistance exercise training and successive detraining on body composition, lipid profile, muscle strength, oxidative stress, and inflammatory markers of postmenopausal breast cancer survivors undergoing tamoxifen treatment.

NCT ID: NCT04478669 Completed - Clinical trials for Invasive Breast Cancer

Digital Breast Tomosynthesis (DBT) to Improve Assessment of Resection Margins in Invasive Breast Cancer

DBT
Start date: September 17, 2020
Phase:
Study type: Observational

The challenge of breast conserving surgery (BCS) is to obtain free resection margins, by removing the invasive tumor and the precursor cells: DCIS (Ductal Carcinoma in Situ). Consequently, 17%-25% of primary invasive breast cancer patients will need a repeat surgery. Repeat breast surgery has been associated with higher surgical risks, poorer cosmetic outcome and increased psychological and economic burden. Finding a precise method to obtain tumor- and DCIS-free resection margins during BCS is therefore strongly needed. The purpose with this study is to investigate if the need for a re-operation can be reduced by performing Digital Breast Tomosynthesis (DBT) of the resected tumor margins compared to the currently used standard X-ray during BCS.

NCT ID: NCT04477616 Completed - Breast Cancer Clinical Trials

Injection Regimen Trial of PEG-rhG-CSF During Breast Cancer Chemotherapy

Start date: July 13, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to try to find a better injection regimen (including time and dose) of PEG-rhG-CSF, which is supposed to better prevent bone marrow suppression and/or FN in breast cancer patients who receive chemotherapy.