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Breast Neoplasms clinical trials

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NCT ID: NCT00156052 Completed - Breast Cancer Clinical Trials

Hypofractionated Radiotherapy Post-Lumpectomy in Women With Node Negative Breast Cancer

Start date: April 1993
Phase: N/A
Study type: Interventional

To determine if hypofractionated radiotherapy to the whole breast (4,250 cGy/16 fractions over 22 days) is equally effective to standard fractionated radiotherapy (5,000 cGy/25 fractions over 35 days) in women with node negative breast cancer who have undergone lumpectomy. The primary outcome is local breast recurrence and secondary outcomes include morbidity and cost effectiveness.

NCT ID: NCT00156039 Completed - Breast Cancer Clinical Trials

Randomized Trial of Follow-up Strategies in Breast Cancer

Start date: January 1997
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether family physician 'routine follow-up care' of women with breast cancer in remission is an acceptable alternative to the existing system of specialist follow-up. Primary outcome measure are event rates of oncological catastrophes and quality of life.

NCT ID: NCT00155259 Completed - Breast Cancer Clinical Trials

Docetaxel, Cisplatin and Capecitabine as Neoadjuvant Chemotherapy for Locally Advanced Breast Cancer

Start date: October 2004
Phase: Phase 2
Study type: Interventional

The primary endpoint of this phase II trial is the objective response rate of the regimen. The secondary endpoints include treatment-related toxicity, progression free survival and overall survival and breast conserving rate.

NCT ID: NCT00155090 Recruiting - Breast Neoplasms Clinical Trials

Proton Magnetic Resonance Spectroscopy of Normal Breast Tissues in Women Volunteers

Start date: January 2005
Phase: N/A
Study type: Observational

Magnetic resonance spectroscopy (MRS) is a diagnostic technique in MRI that distinguishes various metabolites on the basis of their slightly different chemical shifts or resonance frequencies. The Proton is the most abundant nucleus in the body. We will try to establish the typical proton MRS pattern of normal women breasts to be a guideline for future further investigations.

NCT ID: NCT00155038 Recruiting - Breast Cancer Clinical Trials

Imaging Characteristics of Breast Cancer in Women Under 40 Years of Age

Start date: January 1998
Phase: N/A
Study type: Observational

To evaluate if there is any imaging characteristic of breast cancers in women younger than 40 years of age.

NCT ID: NCT00154882 Recruiting - Breast Cancer Clinical Trials

Paclitaxel (Phyxol) and Cisplatin as First-line Chemotherapy for Metastatic Breast Cancer

Start date: September 2003
Phase: Phase 2
Study type: Interventional

The primary endpoint of this phase II trial is the objective response rate of the stage I (low-dose) regimen. The secondary endpoints include treatment-related toxicity, the change in quality of life, progression free survival and overall survival.

NCT ID: NCT00153907 Completed - Breast Cancer Clinical Trials

Navelbine and Capecitabine in the Treatment of Metastatic Breast Cancer

Start date: March 2002
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find the highest dose of capecitabine and oral navelbine that can be given without causing severe side effects, and to determine the safety, tolerability, and effects (good and bad) of capecitabine given with oral navelbine to patients with advanced breast cancer.

NCT ID: NCT00153894 Completed - Breast Cancer Clinical Trials

Effects of Exercise Intervention on Insulin Levels in Breast Cancer Survivors

Start date: December 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an exercise program comprised of strength and endurance training will lower fasting insulin levels in a group of breast cancer survivors. Insulin may be involved in the risk of breast cancer recurrence.

NCT ID: NCT00153218 Completed - Breast Cancer Clinical Trials

An Observational Study of Current Practice Pattern on the Treatment of Women With Metastatic Breast Cancer Whose Tumors Overexpress Her2neu

Start date: June 2004
Phase: N/A
Study type: Observational

The purpose of this study is to observe clinical outcomes of metastatic breast cancer patients whose tumors overexpress the Her2neu protein and are being treated with trastuzumab (Herceptin)either alone or combination with chemotherapy or hormonal therapy.

NCT ID: NCT00152191 Completed - Breast Cancer Clinical Trials

A Randomized Controlled Study of Postoperative Adjuvant Therapy of Uracil-tegafur (UFT) Compared With Cyclophosphamide/Methotrexate/5-fluorouracil (CMF) in Breast Cancer (NSAS-BC)

Start date: October 1996
Phase: Phase 3
Study type: Interventional

This is a randomized controlled study designed to evaluate the relapse-free survival of the UFT group compared with the CMF group. Patients will be randomly assigned to receive either CMF or UFT within 12 weeks after curative resection. To evaluate treatment efficacy, data on recurrence, and survival will be collected for up to 10 years after enrollment of the final patient. To assess safety, data on adverse events will be collected for 2 years after the start of treatment. Patients'quality of life will be assessed by means of a questionnaire.