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Breast Neoplasms clinical trials

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NCT ID: NCT04431674 Completed - Breast Cancer Clinical Trials

Novel MRI-Guided Ultrasound Stimulated Microbubble Radiation Treatment for Patients With Chest-wall and Breast Cancer

USmBRT-B
Start date: July 22, 2020
Phase: Phase 1
Study type: Interventional

The objective of this study is to demonstrate the feasibility of novel MRI-guided ultrasound stimulated microbubble treatment to enhance radiation effects in humans receiving external beam radiotherapy delivered using a LINAC (linear accelerator) radiation therapy device.

NCT ID: NCT04426435 Completed - Breast Cancer Clinical Trials

Effects a Honey Based Syrup on Blood Parameters in Patients With Breast Cancer

Start date: June 15, 2020
Phase: Phase 2
Study type: Interventional

Study aim Determination of the effect of a honey based (HB) syrup on the blood parameters of patients with breast cancer Design Two arm parallel group randomised clinical trial, double blinded Settings and conduct Design of the study: Women patients with breast cancer referring to Shohaday-e- Tajrish Hospital of Tehran who are under chemotherapy treatment. In order to blind the investigator, medications are named as "A" for syrup of HB and B for placebo. The patients don't aware of the type of drug they are assigned to. In addition, the groups are entered into statistical analysis as "A" and "B. The patients will revive either A or B syrup for 4 weeks. At the beginning of the trial demographic data would be gathered. Also, a blood sample would be drawn at the beginning time and after the end of intervention period (week 4). Data would be analysed by SPSS software using T-test.

NCT ID: NCT04420598 Completed - Brain Metastases Clinical Trials

DS-8201a for trEatment of aBc, BRain Mets, And Her2[+] Disease

DEBBRAH
Start date: May 25, 2020
Phase: Phase 2
Study type: Interventional

This is a multicenter, international, open-label, single-arm, multicohort, two-stage optimal Simon's design, phase II clinical trial

NCT ID: NCT04418089 Completed - Breast Cancer Clinical Trials

Simvastatin Effect in Combination With Neoadjuvant Chemotherapy to Clinical Response and Tumor-Free Margin in Locally Advanced Breast Cancer

Start date: January 15, 2018
Phase: Phase 2
Study type: Interventional

Introduction: Neoadjuvant chemotherapy (NACT) has been the standard therapy for treating patients with locally advanced breast cancer (LABC). Doxorubicin-based regimen showed a clinical response for 70-80%. However, the cardiotoxicity from it was not tolerable. Simvastatin acts synergistically with doxorubicin against MCF-7 cells, through downregulation of the cell cycle or induction of apoptosis. Also, it alleviates doxorubicin cardiotoxicity by attenuating ER stress and activating the Akt pathway. Hmgcris a new pathway mediating doxorubicin-induced cell death, and cholesterol control drugs combined with doxorubicin could enhance efficacy and reduce side effects. This study is conducted to see the combination simvastatin and CAF would increase the NACT response and surgical margin of LABC patients. Methods: This study was a double-blind, randomized placebo-controlled trial, conducted in dr. Cipto Mangunkusumo General Hospital and Koja General Hospital. A total of 70 LABC patients were assessed for eligibility. Patients received either a combination of CAF-Simvastatin (40 mg/day) or CAF-Placebo. The biopsy was taken pre-NACT to make the histopathological diagnosis and examine the expression of HMG-CoA Reductase (Hmgcr) and P-glycoprotein (P-gp). Patients were evaluated for the clinical response after 3 cycles. If the response was positive, patients will proceed to surgery. Then, the post-operative specimen will be reviewed for the pathological response. However, if it was a negative response, patients will be given 2nd line NACT.

NCT ID: NCT04414033 Completed - Breast Cancer Clinical Trials

Bubble: A New VR-AI Way of Treatment for Hot Flashes in Women With Breast Cancer

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

This study evaluates the potential of a unique artificial intelligence-virtual reality intervention called Bubble, to reduce the number and intensity of hot flashes and their accompanying psychological symptoms in women, aged 28-55, with breast cancer. A sample of 37 women with breast cancer were selected to the study. Participants were asked to answer a survey before and after using Bubble. The treatment period was 24 days. The findings are positive and show that the use of Bubble help to reduce several psychological symptoms connected to hot flashes.

NCT ID: NCT04411966 Completed - Clinical trials for Metastatic Breast Cancer

Early Interim 18F-FDG-PET and 18F-FLT-PET for Predicting Treatment Response and Survival in Metastatic Breast Cancer

Start date: January 1, 2014
Phase: N/A
Study type: Interventional

We aim to investigate the value of 3'-deoxy-3'-18F-fluorothymidine (18F-FLT) and 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT) for early prediction of treatment response and survival in patients with metastatic breast cancer after salvage therapy.

NCT ID: NCT04408560 Completed - Clinical trials for Breast Cancer Female

Evaluation of the Efficacy of a Homeopathic Protocol in Patients With Non-metastatic Breast Cancer

ARHOMA2
Start date: September 13, 2018
Phase: N/A
Study type: Interventional

Interventional, randomised, prospective, monocentric study

NCT ID: NCT04408118 Completed - Clinical trials for Metastatic Breast Cancer

First Line Atezolizumab, Paclitaxel, and Bevacizumab (Avastin®) in mTNBC

ATRACTIB
Start date: October 5, 2020
Phase: Phase 2
Study type: Interventional

This is a multicenter, open-label, single-arm, phase II clinical trial to evaluate to evaluate the efficacy and safety of first line atezolizumab in combination with paclitaxel and bevacizumab (Avastin®) in patients with advanced or metastatic triple-negative breast cancer (mTNBC)

NCT ID: NCT04406779 Completed - Breast Cancer Clinical Trials

The Frequency of Thyroid Diseases in Women With Breast Cancer

Start date: March 1, 2016
Phase:
Study type: Observational

Breast cancer and thyroid disorders are important health challenges commonly encountered in women. The relationship between both conditions still remains unknown. In this study, the frequency of thyroid diseases was investigated in breast cancer patients

NCT ID: NCT04400552 Completed - Cancer of Breast Clinical Trials

Perioperative Oral Nutrition Supplementation in Malnourished Surgical Cancer Patients

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

The aim of this study is to evaluate the effectiveness of perioperative oral nutrition supplementation (ONS) on nutritional status in malnourished cancer patients undergoing elective surgery. The hypothesis is pre-operative ONS feeding in malnourished surgical cancer patients is effective on improving nutritional status. An extended period of 3 months post-operative ONS feeding is effective on improving nutritional status as compared to ONS feeding post-operatively during hospital stay only. Perioperative feeding is effective on improving secondary outcomes such as sleep quality, post-operative complications and length of hospital stay.