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Bone Marrow Diseases clinical trials

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NCT ID: NCT01561755 Terminated - Clinical trials for HIV-associated Myelopathy

A Double-Blind, Placebo Controlled Study of Intravenous Immunoglobulin for HIV-Associated Myelopathy

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether Intravenous Immunoglobulin (IVIG) is an effective treatment for HIV associated myelopathy.

NCT ID: NCT01511445 Completed - Myelopathy Clinical Trials

Interbody Fusion Devices in the Treatment of Cervicobrachial Syndrome

CASCADE
Start date: December 2011
Phase: N/A
Study type: Interventional

This study randomizes neck and arm pain patients being treated with discectomy and anterior interbody fusion into two groups: one to receive a new ceramic implant and a control group with a more traditional plastic implant. The study will measure and compare pain and disability improvement with the two products over a period of two years. The fusion status will also be judged with plane x-rays and one CT scan.

NCT ID: NCT01511289 Completed - Leukemia Clinical Trials

Radotinib Versus Imatinib in Newly Diagnosed Philadelphia Chromosome and Chronic Myeloid Leukemia Chronic Phase Patients

Start date: August 2011
Phase: Phase 3
Study type: Interventional

In this study, the efficacy and safety of two radotinib doses, 300 mg twice daily and 400 mg twice daily, will be compared with imatinib 400 mg once daily in newly diagnosed patients with Philadelphia chromosome-positive (Ph+) Chronic Myelogenous Leukemia in the chronic phase (CML-CP).

NCT ID: NCT01470105 Active, not recruiting - Bone Metastases Clinical Trials

Improving a Bayesian Model's Survival Estimates in Patients Needing Surgery for Bone Metastases

Start date: November 2011
Phase:
Study type: Observational

The goal of this study is to improve how we estimate survival of people with cancer that has spread to their bone. There have been previous attempts to estimate survival of people with cancer that spread to the bone, but they have not been accurate. This study will try to improve the way we estimate survival in people with cancer that has spread to their bone by looking to see if a physician assessment and a patient assessment of the health status can be blended to give a better estimate of survival than patients or doctors alone.

NCT ID: NCT01440452 Terminated - Clinical trials for Inflammatory Myelopathies

CNS Growth Factors Release and Changes in the Inflammatory Environment in Response to Electrical Stimulation in Subjects With Inflammatory Myelopathies

FIRST-STIM
Start date: November 2010
Phase: N/A
Study type: Interventional

This research is being done to see how different amounts of Functional Electrical Stimulation (FES) affect cycling on factors in blood and spinal cord in people with spinal cord inflammation.

NCT ID: NCT01429493 Completed - Bone Metastases Clinical Trials

Biological Image Guided Antalgic Stereotactic Body Radiotherapy of Bone Metastases

Start date: February 2013
Phase: Phase 2/Phase 3
Study type: Interventional

In various common cancers, the skeleton is a preferred site of metastasis. These bone metastases are the most common cause of cancer-related pain, which significantly impair quality of life. It is postulated that the clinical target volume (CTV) of painful bone metastases consists of cancer cells and tumor-associated host cells: the tumor-host ecosystem. Advances in biological imaging (positron emitting tomography PET) might allow us to selectively identify the tumor-host ecosystem within the anatomical boundaries of a bone metastasis. These findings suggest the potential of intentionally non-homogenous dose escalation (dose painting by numbers) to improve pain control. The hypothesis is that fluorodeoxyglucose positron emitting tomography (FDG-PET) can detect the intra-bone metastasis regions confined with tumor-associated host-cell compartments responsible for metastasis-related pain. The primary objective is to improve pain control with biological image-guided stereotactic body radiotherapy compared to conventional radiotherapy.

NCT ID: NCT01428219 Terminated - Clinical trials for Prostate Cancer Metastatic

Trial of Cabozantinib (XL184) in Castrate-Resistant Prostate Cancer Metastatic to Bone

Start date: February 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to look at the effects of cabozantinib on castrate-resistant prostate cancer metastatic (cancer that has spread to other parts of the body) to the bone and to learn about any side effects caused by taking cabozantinib.

NCT ID: NCT01419717 Completed - Clinical trials for Bone Metastases in Subjects With Advanced Breast Cancer

Open-Label Access Protocol of Denosumab for Subjects With Advanced Cancer

Start date: November 22, 2011
Phase: Phase 3
Study type: Interventional

This trial will facilitate access to denosumab for adults with advanced cancer who have participated in a denosumab phase 3 study until denosumab is approved and available for sale.

NCT ID: NCT01417403 Terminated - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Hydroxychloroquine in Treating Patients With Solid Tumors Undergoing Radiation Therapy for Bone Metastases

Start date: August 2011
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of hydroxychloroquine in treating patients with solid tumors undergoing radiation therapy for bone metastases. Drugs, such as hydroxychloroquine, may make tumor cells more sensitive to radiation therapy

NCT ID: NCT01409720 Completed - Clinical trials for Vertebral Bony Metastases

Isometric Muscle Training in Patients With Spinal Bony Metastases Under Radiation Therapy

DISPO
Start date: September 2011
Phase: Phase 2
Study type: Interventional

Standard indications for palliative radiation of bony metastases include pain, spinal cord compression, and impending pathologic fractures. Palliative radiation therapy serves to reduce pain, improve quality of life, and avoid complications. Tailored training of the paravertebral musculature may support radiation therapy and improve above named factors. DISPO was designed to investigate the impact of tailored physical exercise in patients with vertebral metastases as compared to manual therapy (massage etc.). The trial includes patients with painful bony metastases, patients with spinal cord compression or impending pathological fractures are excluded. The investigations are carried out in a prospective randomized controlled phase-II parallel group design.