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Breast Cancer clinical trials

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NCT ID: NCT04518085 Completed - Breast Cancer Clinical Trials

Psychological Interventions to Prevent Late Effects in Breast Cancer

PREVENT
Start date: October 1, 2020
Phase: N/A
Study type: Interventional

The study aims to investigate whether a combined pre-operative medical hypnosis plus a post-operative internet-based acceptance and commitment intervention are more effective in preventing post-surgical pain and fatigue following breast cancer surgery compared with pre-operative mindfulness plus treatment as usual.

NCT ID: NCT04517370 Completed - Breast Cancer Clinical Trials

CO2 Laser Therapy for the Treatment of GSM in Patients With Breast Cancer

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

Given the need for an effective, non-hormonal treatment for Genitourinary syndrome of menopause GSM) symptoms in breast cancer survivors, the reported efficacy of fractional CO2 laser as such a treatment in retrospective studies, the study aims to evaluate the efficacy of CO2 laser for the treatment of GSM in breast cancer patients, in a prospective, randomized, blinded, placebo-controlled trial.

NCT ID: NCT04517318 Completed - Breast Cancer Clinical Trials

Treatment After Palbociclib-containing Regimens

Start date: August 15, 2017
Phase:
Study type: Observational

To evaluate the prescription patterns and treatment outcomes of subsequent therapies after progression on palbociclib in the real world.

NCT ID: NCT04517305 Completed - Breast Cancer Clinical Trials

Pyrotinib Plus Vinorelbine in HER2+ Metastatic Breast Cancer Patients

Start date: May 15, 2018
Phase:
Study type: Observational

To evaluate the patterns and treatment outcomes of pyrotinib plus vinorelbine in the real world.

NCT ID: NCT04515888 Completed - Breast Cancer Clinical Trials

Evaluation of the Prevalence of Pelvic Static Disorders in Women With Localized Breast Cancer

STATICBREAST
Start date: September 18, 2020
Phase:
Study type: Observational

In this study, investigator propose to assess the prevalence of pelvic static disorders in women undergoing adjuvant hormone therapy for localized breast cancer and to assess the overall quality of life in these patients

NCT ID: NCT04514159 Completed - Breast Cancer Clinical Trials

A Study of ZN-c5 and Abemaciclib in Participants With Breast Cancer

Start date: November 12, 2020
Phase: Phase 1
Study type: Interventional

This is a Phase 1b, open-label, multicenter, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of ZN-c5 administered orally in combination with abemaciclib (VERZENIO®) in participants with advanced estrogen-receptor positive, human epidermal growth factor receptor-2 negative (ER+/HER2-) breast cancer.

NCT ID: NCT04512391 Completed - Breast Cancer Clinical Trials

Analgesic Efficacy of Erector Spinae Plane Block After Breast Cancer Surgery

Start date: September 1, 2018
Phase:
Study type: Observational

Erector spinae plane block(ESPB), which is firstly used for thoracic neuropathic pain, is newly developed and highly promising fascial plane block for providing postoperative analgesia for a great deal of surgeries including breast surgery. The investigators aim to study efficacy of ESPB for patients who undergone breast cancer surgery and is expected to benefit from opioid-sparing effect of this technique.

NCT ID: NCT04511832 Completed - Breast Cancer Clinical Trials

Comparative Effectiveness of Acupuncture and Nonsteroidal Anti-inflammatory Drugs for the Management of Aromatase Inhibitor Induced Arthralgia Among Breast Cancer Survivors

Start date: March 28, 2018
Phase: N/A
Study type: Interventional

Hormone therapy is used to treat women with hormone receptor-positive breast cancer and aromatase inhibitor (AI) is administered after menopause. AI therapy has been proven to be effective in improving the disease-free survival rate, decreasing the recurrence rates and a lower incidence of contralateral breast cancer. However, arthralgia frequently reported as an important adverse event of AI therapy and sometimes resulted in noncompliance with AI therapy. The prevalence of AI induced arthralgia rates ranged from 20 to 74%. Inadequately managed AI induced arthralgia remains a major unmet need in oncology practice in breast cancer survivors. The goal of this project is to conduct a crossover designed pragmatic clinical trial to evaluate the effectiveness of acupuncture versus NSAID (Diclofenac) for the management of aromatase inhibitor induced arthralgia. The third group was set to use non-steroidal analgesics plus acupuncture to evaluate the effectiveness of joint pain.

NCT ID: NCT04509284 Completed - Breast Cancer Clinical Trials

Analgesic Effect of Resistance Training for Breast Cancer Survivors

(ANTRAC)
Start date: August 10, 2020
Phase: N/A
Study type: Interventional

Persistent pain after treatment for breast cancer is a major clinical problem, affecting 25-60 % of the patients and is a source of considerable physical disability and psychological distress. Thus, the development of novel interventions to improve pain management for these patients is of clinical importance. Resistance training (RT) is a promising tool to combat a variety of undesirable adverse effects due to breast cancer treatment. Further, research suggests that it may also be able to provide pain-relieving benefits. Hypothesis: Resistance training will improve pain perception and physical function in the short- and long term compared to a non-training control group.

NCT ID: NCT04504201 Completed - Breast Cancer Clinical Trials

Patient-centered Communication About Healthy Weight in Early Breast Cancer

Start date: June 15, 2020
Phase:
Study type: Observational

Comorbidities in breast cancer survival account for 49% of overall survival difference between black and white women. Many obesity-related comorbidities disproportionately affect black women, therefore pointing to a need to address obesity related comorbidities in survival disparities in early breast cancer patients. This study tinvestigates how messages and messaging about healthy weight can be tailored for racially diverse breast cancer survivors with obesity in order to ensure that clinic-based communications between patients and their oncology provider are patient-centered and culturally sensitive.