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NCT ID: NCT00805012 Terminated - Clinical trials for Head and Neck Squamous Cell Carcinoma

Docetaxel and S-1 in Head and Neck Squamous Cell Carcinoma (HNSCC)

Start date: December 2008
Phase: Phase 2
Study type: Interventional

To assess response rate of docetaxel and S-1 combination in metastatic or recurrent head and neck squamous cell carcinoma

NCT ID: NCT00804310 Terminated - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Lapatinib and Ixabepilone in Treating Patients With Advanced Solid Tumors

UCDCC#207
Start date: August 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Lapatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as ixabepilone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving lapatinib together with ixabepilone may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of lapatinib given together with ixabepilone in treating patients with advanced solid tumors.

NCT ID: NCT00802269 Terminated - Clinical trials for Proliferative Diabetic Retinopathy

Pain Using Reduced Fluence Parameters in Photocoagulation for Diabetic Retinopathy.

Start date: March 2008
Phase: Phase 4
Study type: Interventional

The used of reduced fluence parameters for panretinal photocoagulation decreases pain as perceived by the patient, compared to traditional parameters.

NCT ID: NCT00801775 Terminated - Clinical trials for Peritoneal Dialysis-associated Peritonitis

Improved Diagnosis of Peritoneal Dialysis Peritonitis by Calorimetry

Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study is to analyze whether calorimetry compared to conventional methods (i.e.blood culture systems)is superior to diagnose peritoneal dialysis related peritonitis.

NCT ID: NCT00800150 Terminated - Lymphoma Clinical Trials

Total Marrow and Total Lymph Node Irradiation, Fludarabine, and Melphalan Followed By Donor Stem Cell Transplant in Treating Patients With Advanced Hematological Cancer That Has Not Responded to Treatment

Start date: November 2008
Phase: Phase 1
Study type: Interventional

RATIONALE: Giving total marrow and total lymph node irradiation together with low doses of chemotherapy before a donor stem cell transplant helps stop the growth of cancer cells. It may also stop the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). PURPOSE: This phase I trial is studying the side effects and best dose of total marrow and total lymph node irradiation when given together with fludarabine and melphalan followed by donor stem cell transplant in treating patients with advanced hematological cancer that has not responded to treatment.

NCT ID: NCT00799773 Terminated - Clinical trials for Thrombotic Thrombocytopenic Purpura

Evaluating the Effectiveness of Adding Rituximab to Standard Treatment for Thrombotic Thrombocytopenic Purpura (TTP)

STAR
Start date: April 2009
Phase: Phase 3
Study type: Interventional

Thrombotic thrombocytopenic purpura (TTP) is a rare disorder that causes blood clots to form in blood vessels. The main treatment for TTP is plasma exchange, in which affected patients receive transfusions of plasma, the liquid part of blood, from healthy donors. This study will examine the effectiveness of an antibody, rituximab, in combination with plasma exchange, at improving the immune response in people with TTP and decreasing the recurrence of TTP.

NCT ID: NCT00798525 Terminated - Clinical trials for Heparin Induced Thrombocytopenia (HIT)

Argatroban Versus Lepirudin in Critically Ill Patients

ALiCia
Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test the hypotheses that argatroban significantly increases efficacy and safety of renal replacement therapy measured as life time of haemodialysis filters as compared to lepirudin

NCT ID: NCT00797550 Terminated - Clinical trials for Single Level Posterolateral Spinal Fusion

Use of TRC Autologous Bone Marrow Cells in Posterolateral Lumbar Spine Fusion

Start date: April 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The hypothesis is that Aastrom TRC autologous bone marrow tissue "grafts" can be safely used to promote bone healing as part of a single level posterolateral spine fusion surgical procedure.

NCT ID: NCT00797043 Terminated - Clinical trials for Malignant Neoplasm of Skin Head and Neck

Photon/Proton Radiation Therapy for Carcinoma of the Skin of the Head and Neck

SK01
Start date: September 2008
Phase: N/A
Study type: Observational

The purpose of this study is to collect information from the questionnaire and your medical records to see what effects the proton radiation has on you and your cancer and collect and analyze morbidity outcomes: Incidence of xerostomia (dry mouth) and tumor control.

NCT ID: NCT00796419 Terminated - Clinical trials for Respiratory Distress Syndrome, Acute (ARDS)

Comparative Evaluation of Albumin and Starch Effects in Acute Lung Injury (ALI)

CEASE
Start date: January 2009
Phase: Phase 3
Study type: Interventional

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are similar conditions in which the lungs are critically injured by another inflammatory process in the body. Together they affect more than 150,000 people per year in the United States, with mortality approaching 50% and a financial burden estimated to exceed $5 billion. Fluid overload, weight gain, and reduced oncotic pressure (low blood proteins) are associated with prolonged need for mechanical ventilation and mortality in patients with ALI/ARDS. Historical studies have provided conflicting evidence for benefits with colloid or diuretic therapy in ALI/ARDS, but recent clinical trials have demonstrated significant improvements in blood oxygen levels. The mechanisms of these benefits are not yet certain, but appear to relate to albumin's (a protein medicine) specific ability to influence injury and inflammation in the lungs, thus improving the ability for the lung to repair and exchange oxygen. The purpose of this project is to determine the effects of therapies that affect blood proteins on their ability to change the way the lungs and cardiovascular system (heart and blood vessels) function. Special measurements will be taken to understand how these protein medicines change the ability of the lung and whole body to recover from widespread injury, with additional measures of specific heart and lung function. This clinical trial randomizes ALI/ARDS patients with low blood protein levels to receive albumin (a natural blood protein that is known to influence inflammation) or hetastarch (a synthetic blood protein) with diuretic therapy targeted to improve respiratory function. Therapeutic effects on respiratory function and blood oxygen levels, extravascular lung water, oncotic pressure, lung fluid removal, and heart function will be characterized. This trial will advance our understanding of treatment of ALI/ARDS and the factors that affect fluid balance in the lungs of these patients. Funding Source - FDA OOPD