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Bone Metastasis clinical trials

View clinical trials related to Bone Metastasis.

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NCT ID: NCT02426697 Recruiting - Bone Metastasis Clinical Trials

Pain Management With Pecfent in the Prevention of Pain Induced by Position in Radiotherapy

PARABONE
Start date: May 2015
Phase: Phase 3
Study type: Interventional

The clinical trial is a stage 3 study to determine the role of fentanyl transmucosal in the prevention of pain induced by mobilization in patients receiving a bone metastasis radiation for bone metastasis irradiations

NCT ID: NCT02293642 Completed - Bone Metastasis Clinical Trials

Bone Pain Score Validation Initiative

ARIE
Start date: December 2014
Phase:
Study type: Observational

Translation and validation of the BOMET-QoL-10 questionnaire in Germany and assessment of its validity and responsiveness.

NCT ID: NCT02231476 Recruiting - Clinical trials for Gastrointestinal Cancer

Efficacy of Radiotherapy in Combination With Zoledronic Acid on Pain Relief in Bone Metastasis Patients

Start date: November 2014
Phase: Phase 2
Study type: Interventional

Bone metastasis causes bone destruction and skeletal related events (SRE) including compression fracture, hypercalcemia, and spinal cord compression. Therefore, palliative treatments for pain control and local control have become important and multidisciplinary multimodality approach is needed for treatment of bone metastasis. The efficacy of radiotherapy (RT) for bone metastasis is well known. And the results that bisphosphonate decreases SRE in patients with solid tumor and multiple myeloma reported. In previous retrospective reports, the combination of local RT and systemic bisphosphonate was more effective than RT alone. Therefore, the investigators designed a phase II study to evaluate the efficacy of RT in combination with zoledronic acid on pain relief and the safety of RT in bone metastasis patients with gastrointestinal tumors.

NCT ID: NCT02011880 Temporarily not available - Breast Cancer Clinical Trials

Standardization Research of TCM Syndrome Differentiation and Treatment on Advanced Breast Cancer

Start date: n/a
Phase: N/A
Study type: Expanded Access

The purpose of this clinical research study is to learn if the clinical effects of combined Chinese herbal medicine with endocrine therapy is better than endocrine therapy alone in improving the quality of life and shrinking and slowing the growth of the cancer in women with breast cancer bone metastasis.

NCT ID: NCT01998607 Completed - Solid Tumours Clinical Trials

Survey of XGEVA® Presrcibers in Europe to Evaluate Their Knowledge of the Summary of Product Characteristics Pertaining to Osteonecrosis of the Jaw

Start date: February 4, 2013
Phase: N/A
Study type: Observational

Osteonecrosis of the Jaw (ONJ) is an adverse effect of antiresorptive therapy that is well-recognized in patients with advanced cancer. Detailed information regarding this risk is specified in the Summary of Product Characteristics (SPC). The statements in the SPC are the most important mechanism for minimizing the risk for ONJ. The study objective is to measure the knowledge of oncology practitioners prescribing XGEVA® regarding the content pertaining to ONJ in the SPC after commercial availability.

NCT ID: NCT01833806 Completed - Bone Metastasis Clinical Trials

A Phase IV Post Approval Clinical Study of ExAblate Treatment of Metastatic Bone Tumors for the Palliation of Pain

Start date: September 2013
Phase: N/A
Study type: Interventional

The study hypotheses is that the proportion of patients experiencing clinically significant pain relief will be at least 30% greater than the proportion experiencing worsening pain.

NCT ID: NCT01784393 Completed - Breast Cancer Clinical Trials

Chemoradiation for Bone Metastasis

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

Pain from bone metastases of breast cancer origin is treated with localized radiation. Modulating doses and schedules has shown little efficacy in improving results. Given the synergistic therapeutic effect reported for combined systemic chemotherapy with local radiation in anal, rectal, and head and neck malignancies, the investigators sought to evaluate the tolerability and efficacy of combined capecitabine and radiation for palliation of pain due to bone metastases from breast cancer Hypothesis: Given the hypothesis that regimens employing greater intensity radiation yield higher rates of pain relief, radiosensitization using a tumor targeted drug like Xeloda should improve the rate of complete pain relief as compared to radiosensitization with 5FU alone. Primary Objective: To determine the frequency and duration of pain relief and narcotic relief for the proposed regimen. Secondary Objective: To determine the toxicity of concurrent Capecitabine and radiotherapy in breast cancer patients with bone metastases.

NCT ID: NCT01765907 Completed - Bone Metastasis Clinical Trials

Antalgic Treatment of Painful Bone Metastases by US-guided High Intensity Focused Ultrasound (HIFU)

Start date: December 2012
Phase: Phase 1
Study type: Interventional

Antalgic treatment of painful bone metastases by US-guided High Intensity Focused Ultrasound (HIFU).

NCT ID: NCT01586273 Terminated - Bone Metastasis Clinical Trials

Multicenter Study of Magnetic Resonance-guided High Intensity Focused Ultrasound for Pain Palliation of Bone Metastases

Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of the Philips Sonalleve Magnetic Resonance Imaging-guided High Intensity Focused Ultrasound (MR-HIFU) device for treating painful bone metastases.

NCT ID: NCT01309048 Completed - Bone Metastasis Clinical Trials

Magnetic Resonance-Guided High Intensity Focused Ultrasound for Palliation of Painful Skeletal Metastases

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

This study is to confirm the safety and technical of MRI guided High Intensity Focused Ultrasound (HIFU) for Palliation for Pain of Skeletal Metastases. MRI guided high intensity focused ultrasound uses ultrasound to heat and thermally ablate tissue. The MRI system identifies the ultrasound path and monitors heat rise in the tissue. The goal of the study is to show treatment safety and effectiveness. MR-guided HIFU will be performed in patients who pass inclusion/exclusion criteria.