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NCT ID: NCT00770744 Completed - Schizophrenia Clinical Trials

Efficacy of Lu 31-130 in Patients With Schizophrenia

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

The main purpose with the study is to explore the efficacy and safety of Lu 31-130 in patients suffering from schizophrenia compared to a standard antipsychotic drug.

NCT ID: NCT00769067 Completed - Clinical trials for Non-small Cell Lung Cancer

A Randomized Trial Of PF-00299804 Taken Orally Versus Erlotinib Taken Orally For Treatment Of Advanced Non-Small Cell Lung Cancer That Has Progressed After One Or Two Prior Chemotherapy Regimen

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

This study will compare PF-00299804 given orally on continuous schedule to the approved drug, erlotinib, in patients whose non-small cell lung cancer has progressed after chemotherapy; patients will be randomized to receive one of these drugs, and followed for efficacy and tolerance of each.

NCT ID: NCT00768755 Completed - Clinical trials for Carcinoma, Non-Small Cell Lung

Evaluation Of The Efficacy Of The Combination Of Axitinib With Pemetrexed And Cisplatin In The Treatment Of Non-Squamous Non-Small Cell Lung Cancer

Start date: January 2009
Phase: Phase 1/Phase 2
Study type: Interventional

AG-013736 (axitinib) in combination with cisplatin and pemetrexed will be evaluated as first-line treatment of patients with locally advanced, recurrent, or metastatic non-squamous, non small cell lung cancer (NSCLC).

NCT ID: NCT00767806 Completed - Clinical trials for Chronic Low Back Pain

A Study for Patient With Chronic Low Back Pain

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if duloxetine reduces the severity of chronic low back pain.

NCT ID: NCT00767520 Completed - Breast Cancer Clinical Trials

Safety and Efficacy of Exemestane Plus Dasatinib Versus Placebo for Advanced ER+ Breast Cancer

Start date: February 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether exemestane plus dasatinib will be well-tolerated and will increase progression-free survival (PFS) in the treatment of advanced estrogen-receptor positive (ER+) breast cancer after disease progression (PD) on a non-steroidal aromatase inhibitor (NSAI).

NCT ID: NCT00767325 Completed - Clinical trials for Rheumatoid Arthritis

A Rheumatoid Arthritis Study to Assess Early Response to Abatacept+MTX as Defined by Improvement of Synovitis Measures by Power Doppler Ultrasonography

Start date: December 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess early signs of response to abatacept+methotrexate in metacarpophalangeal joints in both hands using power Doppler ultrasonography in patients with active rheumatoid arthritis.

NCT ID: NCT00766350 Completed - Fibromyalgia Clinical Trials

Comparative Efficacy and Tolerability of Quetiapine XR and Amitriptyline in the Treatment of Fibromyalgia

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

Quetiapine, a second generation antipsychotic, has shown beneficial activity on fibromyalgia symptomatology, administered as add-on treatment, in a sample of 35 patients. The purpose of the present study is to compare, in a controlled setting, the efficacy and the tolerability of quetiapine extended release with amitriptyline in the treatment of patients with fibromyalgia

NCT ID: NCT00765830 Completed - Clinical trials for Diabetes Mellitus, Type 2

Safety and Tolerability of Vildagliptin Versus Placebo in Patients With Type 2 Diabetes and Moderate or Severe Renal Insufficiency (28 Week Extension)

Start date: September 2008
Phase: Phase 3
Study type: Interventional

This clinical trial is designed to provide additional information on the safety and tolerability of vildagliptin (50 mg once daily (qd)) when used in patients with type 2 diabetes mellitus (T2DM) and moderate or severe renal insufficiency

NCT ID: NCT00765713 Completed - Sleep Apnea Clinical Trials

Sleep Apnea-hypopnea Syndrome (SAHS) and Ventricular Arrhythmias

SAHS-ICD
Start date: October 2008
Phase: Phase 4
Study type: Interventional

Hypothesis: The CPAP treatment diminishes the effect of ventricular arrhythmias in patients with ischemic heart disease or dilated myocardiopathy, systolic ventricular disfunction and sleep apnea-hypopnea syndrome (SAHS)Objectives: To analyze the incidence of ventricular arrhythmias (premature ventricular beat, non-sustained ventricular tachycardia and sustained ventricular tachycardia) and appropriate defibrillator therapies in patients with ischemic heart disease or dilated myocardiopathy, moderate-severe left ventricular dysfunction,with an implantable cardioverter-defibrillator (ICD) and sleep apnea. To study the effect of CPAP on the cardiac arrhythmias and on the number of appropriate defibrillator therapies. Design: Parallel, randomized and single-blinded multicentric study to compare CPAP vs. hygienic-dietetic recommendations. Patients with SAHS (AHI≄15) and systolic left ventricle dysfunction patients with an ICD. Duration: 24 months.

NCT ID: NCT00765635 Completed - Hearing Loss Clinical Trials

Chlorobutanol, Potassium Carbonate, and Irrigation in Cerumen Removal

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

Accumulation of cerumen in the external ear canal is a common problem. The presence of cerumen not only interferes with the clinician's view of the tympanic membrane, but may also result in hearing loss and vertigo, and may predispose to ear infections. Removal of cerumen is facilitated by the use of a variety of ceruminolytics, or wax solvents. The current study was designed to evaluate the ceruminolytic effects of a single, brief application of the two most frequently used products in the investigators area, containing chlorobutanol or potassium carbonate with or without irrigation in the primary care setting in a randomized, single-blind trial. To our knowledge, this is the first randomized study comparing ceruminolytics with chlorobutanol versus potassium carbonate.