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Breast Cancer clinical trials

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NCT ID: NCT00589043 Not yet recruiting - Breast Cancer Clinical Trials

Computed Tomography Laser Mammography Breast Imaging Device

CTLM
Start date: October 2015
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the sensitivity and specificity of the CTLM system when used adjunctively with mammography compared to mammography alone in the heterogeneously and extremely dense breast population.

NCT ID: NCT00536055 Not yet recruiting - Breast Cancer Clinical Trials

Dyadic Coping in Breast and Prostate Cancer Patients and Their Spouses

Start date: October 2007
Phase: N/A
Study type: Observational

The purpose of this study is to focus on dyadic coping as one of the main factors that enhance resilience in adjustment to cancer, while also assessing other protective factors for coping with traumatic events. Specifically, the study aims are: 1. To assess the level of post traumatic distress, functional impairment and depression among breast and prostate cancer patients and their spouses. 2. To assess resiliency factors such as flexibility, self efficacy and ego resilience among breast and prostate cancer patients and their spouses. 3. To examine the pattern of dyadic coping at 3 time points: at the beginning and end of radiation therapy, and at six-week follow-up. 4. To examine the relationships between dyadic coping and level of posttraumatic distress and the resilience factors over time (in 3 repeated measures) Different aspects of coping with the trauma of cancer and its treatment may be assessed. Measures of strength and distress amongst patients and their spouses may enable a fuller picture of what types of responses exist, which interventions may be most beneficial, and what other factors may relate to positive coping, increased resilience and quality of life, such as flexibility, and the nature of the couples' dyadic coping.

NCT ID: NCT00243165 Not yet recruiting - Breast Cancer Clinical Trials

Lifemel Honey to Reduce Leucopenia During Chemotherapy

Start date: November 2005
Phase: Phase 2
Study type: Interventional

This study will include 60 patients with early breast cancer referred to receive adjuvant chemotherapy with AC ( adriamycin- cyclophosphamide) or CAF ( adriamycin- cyclophosphamide- 5- fluorouracil ) combinations. These patients will receive every day one spoon of Lifemel honey or regular honey ( double blind)- during the adjuvant chemotherapy .Every week a WBC count will be performed in order to record the influence of Lifemel on myelotoxicity.

NCT ID: NCT00173303 Not yet recruiting - Breast Cancer Clinical Trials

The Diagnostic Efficacy of Computer-Aided Detection (CAD) in Full-Field Digital Mammography (FFDM)- A Prospective Study

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of this study is to evalute whether CAD (computer-aided detection) in FFDM (full-field digital mammography) can facilitate the detection rate of breast cancer on mammography compared with FFDM without CAD.