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NCT ID: NCT00648739 Terminated - Multiple Myeloma Clinical Trials

Safety and Dose Ranging Study of Samalizumab to Treat Relapsing or Refractory CLL or MM

Start date: June 19, 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study was to determine the safety and maximum tolerated dose (MTD) of ALXN6000 (samalizumab) in treating relapsing or refractory B-cell chronic lymphocytic leukemia (B-CLL) or multiple myeloma (MM) and to study how samalizumab may help the immune system fight tumors that express CD200.

NCT ID: NCT00646165 Terminated - Clinical trials for B-cell Chronic Lymphocytic Leukemia

Trial of Forodesine in Patients With Relapsed B-cell Chronic Lymphocytic Leukemia

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

To determine the dose and duration of treatment for the best overall response with Forodesine in relapsed B-cell chronic lymphocytic leukemia

NCT ID: NCT00644306 Terminated - Clinical trials for Newly Diagnosed, Multiple Myeloma

Comparison of Melphalan-Prednisone (MP) to MP Plus Thalidomide in the Treatment of Newly Diagnosed Very Elderly Patients (> 75 Years) With Multiple Myeloma

IFM 01/01
Start date: April 2002
Phase: Phase 3
Study type: Interventional

In multiple myeloma, combination chemotherapy with melphalan plus prednisone has been usedsince the 1960s and is regarded as the standard of care in very elderly patients. We assess whether the addition of thalidomide at 100 mg/day to this combination would improve survival.

NCT ID: NCT00643786 Terminated - Clinical trials for Dental Cares Under Kalinox's Inhalation

Interest of Re-oxygenation After Inhalation of 50% Nitrous Oxide / 50% Oxygen Premix in Dental Cares

Start date: February 2004
Phase: Phase 3
Study type: Interventional

The usefulness of re-oxygenation after inhalation of 50% nitrous oxide and 50% oxygen premix (Kalinox 170 bar) during dental care is studied and the pollution resulting from administration of Kalinox is also investigated.

NCT ID: NCT00642824 Terminated - Clinical trials for Non-Squamous Non-Small Cell Lung Cancer

A Genetic Substudy Associated With the Avastin (Bevacizumab) Study MO19390 in Patients With Advanced or Recurrent Non-Squamous Cell Lung Cancer.

Start date: May 2007
Phase: Phase 2
Study type: Interventional

This single arm genetic substudy of MO19390 will test the hypothesis that there is a positive relationship between mRNA BRCAI levels and the response to different chemotherapy combinations plus Avastin. A subset of patients participating in MO19390, and receiving Avastin 15mg/kg iv on day 1 and subsequently once every 3 weeks, will undergo BRCAI mRNA expression determination. Depending on the BRCAI mRNA level (low, medium or high) they will receive a different chemotherapy regimen in combination with Avastin: a)gemcitabine/cisplatin, b)vinorelbine + cisplatin/docetaxel + cisplatin or c)vinorelbine or docetaxel. Avastin treatment will continue after completion of chemotherapy cycles until disease progression, and the target sample size is 100-500 individuals.

NCT ID: NCT00642616 Terminated - Asthma Clinical Trials

Evaluate Safety of Technosphere® Insulin (TI) in Diabetic Subjects With Moderate Obstructive Pulmonary Disease

Start date: March 2009
Phase: Phase 3
Study type: Interventional

Examine the effects of TI in combination with an anti-diabetic regimen including inhaled insulin versus anti-diabetic treatment without inhaled insulin on lung function & pulmonary safety

NCT ID: NCT00640549 Terminated - Clinical trials for Diabetes Mellitus, Type 2

Atorvastatin and LDL Profile in Non-Insulin Dependent Diabetes Mellitus

ALPIN
Start date: March 2003
Phase: Phase 4
Study type: Interventional

The study will investigate the effects of atorvastatin on the concentrations of small, dense LDL and HDL subfractions in patients with diabetes and the underlying mechanisms of these effects.

NCT ID: NCT00640029 Terminated - Kyphosis Clinical Trials

Evaluation of the Prosthetic Disc Replacement

EVA
Start date: February 2008
Phase: N/A
Study type: Interventional

Until now, arthrodesis (intervertebral fusion) is the formal treatment for the lumbar and cervical degenerative disc disease : arthrodesis has been the standard surgical treatment for the patients when nonsurgical management has failed. However , it has shown out some drawbacks : pseudoarthrosis may appear in the short term, and junctional degeneration in the long term. The replacement of the intervertebral disc by a prosthesis (arthroplasty) has been since a few years a major alternative therapeutic to the arthrodesis.: it demonstrates great functional results and less post-interventional complications. It is indicated to restore a normal function of the spine (motion is kept)and to avoid deterioration of the adjacent spinal segments over the long time. In this clinical study, we will distinguish the cervical discal pathology and the lumbar discal pathology. The purpose of this study is to analyze the results of the arthroplasty in terms of functional effects, quality of life, anatomical results and economical results.

NCT ID: NCT00638326 Terminated - Clinical trials for Stable Angina Pectoris

Doubling the Maintenance Dose of Clopidogrel in Patients With High On-Clopidogrel Platelet Reactivity

DOSER
Start date: March 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine whether administration of 150 mg clopidogrel is effective in reducing the one-year incidence of thromboischemic events in patients with high on-clopidogrel platelet reactivity compared to 75 mg clopidogrel after elective percutaneous coronary intervention.

NCT ID: NCT00638053 Terminated - Brain Injuries Clinical Trials

A Study to Evaluate the Efficacy of Somatropin in Adults With Growth Hormone Deficiency Caused by Trauma and/or Head Injury

GHD
Start date: November 2002
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the prevalence of GHD in patients who sustain a head injury or suffer a major traumatic event and to evaluate the efficacy of growth hormone (GH) therapy in the treatment of GHD caused by trauma or head injury