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Breast Neoplasms clinical trials

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NCT ID: NCT03880799 Completed - Breast Cancer Clinical Trials

The MEDITATE-BC Study: Mindfulness-Enhanced Decision Intervention To Aid Treatment Election - Breast Cancer

MEDITATE-BC
Start date: November 8, 2018
Phase: N/A
Study type: Interventional

In this study the investigators propose to pilot test a brief, mindfulness shared decision making intervention that begins shortly after receiving a diagnosis of breast cancer. A mindfulness instructor will conduct an hour long session with consented participants before the scheduled surgical appointment. The investigators hypothesize that a mindfulness intervention delivered shortly after receiving a diagnosis of breast cancer may ultimately lead to increased decisional satisfaction and alignment to participant's values and preferences, and decreased anxiety. To measure this endpoint, participants will complete three surveys via REDCap- at baseline, before surgery, and 6 months postoperatively. Surveys will include questions on quality of life, anxiety, and participant satisfaction with the mindfulness program.

NCT ID: NCT03878823 Completed - Clinical trials for Metastatic Breast Cancer

Safety and Pharmacokinetics of ODM-209

STESIDES
Start date: April 17, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this first-in-human study is to evaluate safety and tolerability of ODM-209 and find the dose of ODM-209.

NCT ID: NCT03874598 Completed - Breast Neoplasm Clinical Trials

Effectiveness of Ear Acupuncture to Improve Insomnia in Women With Breast Cancer

EOMI
Start date: June 12, 2019
Phase: N/A
Study type: Interventional

The aim of this clinical study is to investigate the extent to which ear acupuncture has an effect on insomnia in women with breast cancer. It will be investigated whether changes in sleep quality, fatigue, quality of life, stress, and psychological well-being can be achieved. In addition, a proinflammatory cytokine will be meassured.

NCT ID: NCT03872791 Completed - Clinical trials for Triple-negative Breast Cancer

A Study of KN046 in Subjects With Locally Advanced or Metastatic Triple-negative Breast Cancer

Start date: May 30, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This is an open-label, phase Ib/II, multi-center study to evaluate efficacy and safety of KN046 alone or in combination with nab-paclitaxel in subjects with locally advanced unresectable or metastatic triple negative breast cancer (TNBC). The study is composed of dose escalation and expansion parts. Every subject will subject tumor tissue used for biomarker evaluation. Each subject will receive KN046 or in combination with nab-paclitaxel untill confirmed progressive disease, unacceptable toxicity or withdrawal of informed consent whichever occurs first.

NCT ID: NCT03872388 Completed - Clinical trials for Anatomic Stage III Breast Cancer AJCC v8

Atorvastatin in Treating Patients With Stage IIb-III Triple Negative Breast Cancer Who Did Not Achieve a Pathologic Complete Response After Receiving Neoadjuvant Chemotherapy

Start date: January 14, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well atorvastatin works in treating patients with stages IIb-III triple negative breast cancer who did not achieve a pathologic complete response to neoadjuvant chemotherapy. Pathologic complete response is the lack of all signs of cancer in tissue samples removed during surgery after upfront chemotherapy. Atorvastatin is used for the treatment of high cholesterol and may reduce the risk of triple negative breast cancer from coming back. Triple-negative breast cancer is a type of breast malignancy that is comprised of cancer cells that do not have estrogen receptors, progesterone receptors, or large amounts of HER2/neu protein. Patients with TNBC do not have established systemic therapies such as anti-estrogens or HER2-targeting agents to reduce recurrence after surgery, and residual cancer found at surgery is associated with higher relapse rate.

NCT ID: NCT03872141 Completed - Breast Cancer Clinical Trials

Objective Evaluation of Paclitaxel/Docetaxel-induced Neuropathy in Breast Cancer Patients

Start date: May 23, 2017
Phase:
Study type: Observational

The purpose of this prospective, non-interventional study is to perform neurological and cognitive assessment of breast cancer patients who receive standard of care single agent weekly paclitaxel docetaxel chemotherapy to determine the onset and severity of chemotherapy induced neuropathy (CIPN) and cognitive impairment (CICI).

NCT ID: NCT03868865 Completed - Breast Cancer Clinical Trials

Effects of an Integrative Day-care Clinic Program for Breast Cancer Patients During Chemotherapy

Start date: August 7, 2012
Phase: N/A
Study type: Interventional

The aim of the study was to evaluate a new integrative day-care clinic concept for breast cancer patients receiving chemotherapy. This is an explorative pilot study. Therefore, all outcomes are analyzed exploratively.

NCT ID: NCT03868514 Completed - Breast Cancer Clinical Trials

Post Market Clinical Follow Up to "Patient Reported Outcome" Using a Titanised Polypropylene Mesh (TiLOOP® Bra Pocket)

PRO-Pocket
Start date: July 4, 2019
Phase:
Study type: Observational

"PRO-Pocket" - International prospective multicentre Post Market Clinical Follow Up to "Patient reported outcome" in primary or secondary breast reconstruction after mastectomy using a titanised polypropylene mesh (TiLOOP® Bra Pocket)

NCT ID: NCT03865654 Completed - Breast Cancer Clinical Trials

Individualizing Surveillance Mammography for Older Breast Cancer Survivors

Start date: May 16, 2019
Phase: N/A
Study type: Interventional

This research is being conducted to develop consensus on surveillance mammography and follow-up for breast cancer survivors who are age ≥75.

NCT ID: NCT03862144 Completed - Clinical trials for Chemotherapy-induced Nausea and Vomiting

NEPA to Prevent Chemotherapy Induced Nausea and Vomiting in Patients With Breast Cancer

GIM15-NEPA
Start date: May 12, 2016
Phase: Phase 2
Study type: Interventional

This study evaluates if the activity of one-day of NEPA plus dexamethasone, to prevent chemotherapy-induced nausea and vomiting in breast cancer patients receiving adjuvant AC-based chemotherapy, is maintained during all the chemotherapy cycle treatment (maximum 4 cycles).