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Breast Neoplasms clinical trials

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NCT ID: NCT04045392 Not yet recruiting - Breast Cancer Clinical Trials

Effects of Mediterranean Diet Based Intervention in Breast Cancer Patients

Start date: August 2019
Phase: N/A
Study type: Interventional

The purpose of this randomized clinical trial is to examine the effects of Mediterranean diet based intervention on inflammation and metabolic risk factors in overweight or obese postmenopausal women with breast cancer receiving adjuvant hormone therapy.

NCT ID: NCT04042870 Completed - Breast Cancer Clinical Trials

Effect of Sukshma Vyayama Yoga on Aromatase Inhibitor-Induced Arthralgia in Breast Cancer Survivors

Start date: September 4, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the efficacy of sukshma vyayama joint loosening yoga in improving aromatase inhibitor-induced arthralgia in post-menopausal breast cancer survivors and secondarily, to evaluate the feasibility of delivering the intervention on Facebook.

NCT ID: NCT04042480 Terminated - Colorectal Cancer Clinical Trials

A Study of SGN-CD228A in Advanced Solid Tumors

Start date: September 3, 2019
Phase: Phase 1
Study type: Interventional

This trial will study SGN-CD228A to find out whether it is an effective treatment for different kinds of cancer. It will also look at what side effects (unwanted effects) may occur. The study will have two parts. Part 1 of the study will find out how much SGN-CD228A should be given for treatment and how often. Part 2 of the study will use the dose found in Part 1 and look at how safe and effective the treatment is.

NCT ID: NCT04042051 Terminated - Clinical trials for Metastatic Breast Cancer

Copanlisib in Combination With T-DM1 in Pretreated Unresectable Locally Advanced or Metastatic HER2-positive Breast Cancer

Panthera
Start date: November 12, 2019
Phase: Phase 1
Study type: Interventional

This study is a Phase 1b open label, single arm, adaptive multi-centre trial of copanlisib in combination with trastuzumab emtansine (T-DM1) in pretreated locally advanced or metastatic HER2-positive breast cancer. Patients with unresectable locally advanced or metastatic HER2-positive breast cancer who previously received trastuzumab and a taxane, separately or in combination, will be treated with copanlisib (to the dose escalation scheme) plus trastuzumab emtansine 3.6mg/kg IV on day 1 of a 21-day cycle.

NCT ID: NCT04041128 Completed - Breast Cancer Clinical Trials

PARP Inhibition During Pre-surgical Window in Breast/Ovary Cancer

Start date: July 23, 2019
Phase: Early Phase 1
Study type: Interventional

Study involves surgery for cytoreduction or laparoscopy to determine if you are a candidate for tumor debulking or a tissue biopsy. Following this surgery you will receive chemotherapy. This study will administer 7 days of treatment with a targeted therapy called Lynparza. Lynparza and/or other PARP inhibitors have been FDA approved for the treatment of ovarian and breast cancer. Tissue biopsy will be done before a 7 day course of Lynparza in order to correlate molecular changes to response to treatment. Participation in this trial will require an additional tumor biopsy which will occur either before or after treatment of Lynparza.

NCT ID: NCT04040686 Completed - Breast Cancer Clinical Trials

HER2 Expression Detection in Breast Cancer Using 99mTc-NM-02

Start date: July 29, 2019
Phase: Early Phase 1
Study type: Interventional

A 99mTc-labeled anti-HER2-sdAb (99mTc-NM-02) will be developed for SPECT/CT assessment of HER2 expression in breast cancer patients. Its safety, radiation dosimetry and biodistribution, and the relationship between tumor uptake and HER2 immunohistochemistry results will be investigated.

NCT ID: NCT04040569 Active, not recruiting - Breast Cancer Clinical Trials

A Phase I Dose Escalation Study of Single Fraction Ablative Pre-operative Partial Breast (S-PBI) for Early Stage Breast Cancer

Start date: December 25, 2019
Phase: Phase 1
Study type: Interventional

The purpose of this phase I trial is to evaluate dose-limiting toxicity while dose escalating single-fraction preoperative S-PBI to a presumed radioablative dose over 3 cohorts, starting with 30Gy in 1 fraction and advancing to 34Gy and 38Gy in 1 fraction.

NCT ID: NCT04039893 Recruiting - Clinical trials for Node-positive Breast Cancer

MUltimodal Targeted Axillary Surgery

MUTAS
Start date: October 23, 2019
Phase: N/A
Study type: Interventional

The present trial will prospectively evaluate the accuracy of both a systematic predefined axillary ultrasound imaging together with tumor load quantification of suspicious and sentinel axillary lymph nodes to predict overall tumor load in the axilla.

NCT ID: NCT04039230 Recruiting - Breast Cancer Clinical Trials

Study to Evaluate Sacituzumab Govitecan in Combination With Talazoparib in Patients With Metastatic Breast Cancer.

Start date: October 9, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This research is studying the effect of Antibody-Drug Conjugate Sacituzumab Govitecan in Combination with the Poly (Adenosine Diphosphate [ADP]-Ribose) Polymerase (PARP) Inhibitor Talazoparib in Patients with Metastatic Triple-Negative Breast Cancer.

NCT ID: NCT04038606 Recruiting - Breast Cancer Clinical Trials

SEINIOR:Quality of Life and Breast Cancer in Older Women

SEINIOR
Start date: December 15, 2016
Phase: N/A
Study type: Interventional

Background : Breast cancer is a disease that occurs primarily in elderly women: 54057 of breast cancer occurred on women in 2008, 15.2% were between 75 and 84 years and 5.4% were over 85 years. Elderly women cancers care exposes to several problems: the opportunity for screening, knowing that mammography is not recommended after 75 years old, and the level of treatment depending on the background and the existence of weaknesses. It should determine whether patients are in adequate physiological condition to tolerate classical and "complete" treatment or conversely in a precarious state with advanced fragility, justifying only lightened and adapted symptomatic treatment. Purpose : The purpose of this research theme is to assess the quality of life of elderly patients who underwent mastectomy for breast cancer. The objectives are: - Assess the determinants of acceptance and / or rejection of mastectomy based on personal background (level of fragility, self-image) and linked to cancer - Assess the quality of life, 6 months later, of women who underwent or not mastectomy, and appreciate the determinants Abstract : The total mastectomy allow, oncologically, a more valid treatment than a lumpectomy, in many cases of women suffering from a breast cancer, but its relevance and acceptability are poorly known. Some think that an elderly woman, postmenopausal, is less concerned with her aesthetics and feminine attributes, which would allow her to accept easily the mastectomy. The research hypothesis is that the acceptability of mastectomy is not good in elderly women