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NCT ID: NCT00427323 Suspended - Clinical trials for Sleep Initiation and Maintenance Disorders

Light Exposure to Treat Sleep Disruption in Older People

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether shifts in the timing of the biological clock to a later hour (phase delay shifts of the human circadian system) can be produced in response to four successive evenings of light exposure, and whether that phase shift will result in greater evening alertness and greater nighttime sleep efficiency. Three different light sources will be compared: 1) standard fluorescent light; 2) blue-enriched light; 3) incandescent fluorescent light.

NCT ID: NCT00392106 Suspended - Atrial Fibrillation Clinical Trials

High Intensity Focused Ultrasound (HIFU) Ablation System Study

Start date: April 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the HIFU Pulmonary Vein Ablation System is effective in the treatment of paroxysmal Atrial Fibrillation compared to the control of best medical therapy with FDA approved antiarrhythmic drugs.

NCT ID: NCT00382395 Suspended - Glaucoma Clinical Trials

SOLX Gold Shunt Versus Control Implant: Randomized Trial for Refractory Glaucoma

Start date: November 2005
Phase: Phase 3
Study type: Interventional

Study Objective: To establish the substantial equivalence of the SOLX Gold Shunt to commercially available aqueous shunts, specifically the Ahmed™ Glaucoma Valve Model FP7, in the ability to reduce intraocular pressure (IOP) associated with glaucoma in eyes where medical and conventional surgical treatments have failed.

NCT ID: NCT00353067 Suspended - Clinical trials for Acute Coronary Syndrome

Veliflapon (DG-031)to Prevent Heart Attacks or Stroke in Patients With a History of Heart Attack or Unstable Angina

Start date: May 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if veliflapon (DG-031)can prevent a heart attack or stroke in African American patients with a history of unstable angina or myocardial infarction.

NCT ID: NCT00333307 Suspended - Pre-Eclampsia Clinical Trials

Evaluation of the Safety of Relaxin in Preeclampsia

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether different doses of recombinant human relaxin is safe when given to women with severe preeclampsia

NCT ID: NCT00324831 Suspended - Lymphoma Clinical Trials

GM-CSF With or Without Vaccine Therapy After Combination Chemotherapy and Rituximab as First-Line Therapy in Treating Patients With Stage II, Stage III, or Stage IV Diffuse Large B-Cell Lymphoma

Start date: n/a
Phase: Phase 3
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as cyclophosphamide, doxorubicin, vincristine, and prednisone, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Colony-stimulating factors, such as GM-CSF, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of chemotherapy. Vaccines made from a person's cancer cells may help the body build an effective immune response to kill cancer cells. It is not yet known whether giving GM-CSF together with vaccine therapy is more effective than giving GM-CSF together with a placebo when given after combination chemotherapy and rituximab in treating diffuse large B-cell lymphoma. PURPOSE: This randomized phase III trial is studying GM-CSF and vaccine therapy to see how well they work compared to GM-CSF and placebo when given after combination chemotherapy and rituximab as first-line therapy in treating patients with stage II, stage III, or stage IV diffuse large B-cell lymphoma.

NCT ID: NCT00295230 Suspended - Clinical trials for Respiratory Distress Syndrome

Effects of Volume Guarantee With Pressure Supported vs. Synchronized Intermittent Mandatory Ventilation in VLBW Infants

Start date: February 2006
Phase: Phase 1
Study type: Observational

Studies in preterm infants have shown that adding volume guarantee (VG) to synchronized modes of ventilation is not only feasible but also advantageous for providing more constant and desirable mechanical breath size. This ideally minimizes ventilator-induced lung injury due to barotrauma and volutrauma. To date, only one recent study has investigated the relative advantages of combining VG with different modes of synchronized mechanical ventilation in clinically stable, preterm infants that were mechanically ventilated at an average age of one month. We aim to further evaluate the effects of PSV+VG versus SIMV+VG ventilation in very low birth weight infants within the first three to five days of life. Our hypothesis is that in very low birth weight infants requiring mechanical ventilation in the first three to five days of life, PSV+VG will allow for more stable physiologic and ventilatory parameters compared to SIMV+VG. The primary endpoints are a reduction in respiratory rate and average mean airway pressure in the PSV+VG group compared to the SIMV+VG group.

NCT ID: NCT00280189 Suspended - NSCLC Clinical Trials

Study of Outcomes of Radiofrequency Ablation of Lung Tumors

Start date: September 2003
Phase:
Study type: Observational

The purpose of this study is to assess short and long term outcomes after radiofrequency ablation (RFA) of pulmonary malignancies in patients who are not candidates for surgical resection. This study will evaluate the efficacy of RFA for the treatment of lung tumors by assessing its impact on local tumor control, progression free survival, overall survival, dyspnea score and quality of life (QOL).

NCT ID: NCT00278122 Suspended - Melanoma (Skin) Clinical Trials

Paclitaxel and GM-CSF in Treating Patients With Stage III or Stage IV Melanoma That Cannot Be Removed By Surgery

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

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Biological therapies, such as GM-CSF, may stimulate the immune system in different ways and stop tumor cells from growing. Giving paclitaxel together with GM-CSF may be effective in treating melanoma. PURPOSE: This phase II trial is studying how well giving paclitaxel together with GM-CSF works in treating patients with stage III or stage IV melanoma that cannot be removed by surgery.

NCT ID: NCT00275405 Suspended - Healthy Clinical Trials

Effect of Garlic on Inflammatory Mediators

Start date: April 2006
Phase: Phase 4
Study type: Interventional

This research will investigate the effect of garlic oil extract when added to daily diet on inflammatory mediators and blood clotting activation.