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NCT ID: NCT00971191 Terminated - Clinical trials for Non-Small Cell Lung Cancer (NSCLC)

A Study In Patients Who Will Undergo Surgical Removal Of Non-Small Cell Lung Cancer To Evaluate Molecular Changes That Occur In Tumor Tissue After Short Term Exposure To PF-00299804

Start date: February 2010
Phase: Phase 1
Study type: Interventional

This study will enroll patients who are planned to undergo surgical removal of their tumor. The goal of the study is to evaluate the changes that occur in the tumor after brief (about 8 days) exposure to the study drug.

NCT ID: NCT00970606 Terminated - Influenza Clinical Trials

STIP: Statin Trial for Influenza Patients

STIP
Start date: October 2009
Phase: N/A
Study type: Interventional

To assess the efficacy and safety of oral rosuvastatin in patients with suspected or confirmed influenza who require intensive care unit (ICU) admission due to respiratory distress.

NCT ID: NCT00967642 Terminated - Diabetes Mellitus Clinical Trials

Intravenous Insulin in Patients With Diabetes After Percutaneous Coronary Intervention (PCI)

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

The purpose of this study is to evaluate the effects of intravenous insulin/24 hours to normalize glycemia upon markers of oxidative stress (protein oxidation and total antioxidant defense) and inflammation (C-reactive protein (CRP) and sCD40L) in diabetic patients submitted to PCI with stent.

NCT ID: NCT00965458 Terminated - Clinical trials for New-onset Type 1 Diabetes Mellitus

Inducing Remission in Type 1 Diabetes With Alefacept

T1DAL
Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to test whether a drug called alefacept will slow or halt destruction of the beta cells in the pancreas. If the destruction of the beta cells is stopped, the patients might be able to produce insulin on their own longer, which could stop or slow the progression of their type 1 diabetes. This is a multi-center prospective, placebo-controlled, double-blind and randomized trial to investigate the ability of alefacept to protect residual beta cells from ongoing autoimmune destruction in adolescents and young adults with newly diagnosed Type 1 Diabetes Mellitus (T1DM).

NCT ID: NCT00965419 Terminated - Clinical trials for Attention Deficit Hyperactivity Disorder

A Study of Pediatric Participants With Attention Deficit/Hyperactivity Disorder

Start date: September 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The primary purpose of the study is to assess long-term safety and tolerability of Edivoxetine in pediatric participants with attention deficit hyperactive disorder (ADHD).

NCT ID: NCT00961207 Terminated - Diabetes Clinical Trials

Triple Blockade of the Renin Angiotensin Aldosterone System in Diabetic (Type 1&2) Proteinuric Patients

Start date: August 2009
Phase: Phase 4
Study type: Interventional

Study Hypothesis: Reduction in albuminuria has been shown to decrease progression of diabetic nephropathy. In diabetic nephropathy patients treated with maximal antihypertensive doses with dual RAAS blockade (total daily dose valsartan 320 mg and either enalapril 40 mg or benazepril 40 mg daily, or losartan 100mg), persistent albuminuria reflects further additional RAAS activation. Microvascular renal disease due to increased RAAS activation may be more effectively treated with triple blockade by the addition of a direct renin inhibitor (DRI) Aliskiren.

NCT ID: NCT00959946 Terminated - Clinical trials for Advanced Cholangiocarcinoma (Part 1)

Study Of Bosutinib With Capecitabine In Solid Tumors And Locally Advanced Or Metastatic Breast Cancer

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

This is a research study in 2 parts assessing the following parameters of the combination of the study drug called bosutinib, and a drug called capecitabine: the safety, how well the subject's body handles the study drug, and preliminary anti-tumor activity as treatment for different types of cancers in part 1, and breast cancer only in part 2. In part 1, subjects will receive bosutinib and capecitabine daily at different dose levels of each drug in order to determine the highest tolerated dose of the combination study treatment. In part 2, subjects will receive bosutinib and capecitabine at this highest tolerated dose to see how well the study treatment works to treat breast cancer. In addition, genetic research testing (research analyses involving genes and gene products) will be performed on biological samples from subjects.

NCT ID: NCT00958074 Terminated - Clinical trials for Cutaneous T-cell Lymphoma Stage I

Vorinostat in Patients With Primary Cutaneous T-Cell Lymphoma

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

This phase II trial studies the side effects and how well vorinostat works in treating patients with primary cutaneous T-cell lymphoma. Vorinostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth

NCT ID: NCT00957827 Terminated - Clinical trials for Through-and-through Lip Lacerations

Prophylactic Use of Antibiotics for Through and Through Lacerations of the Lip

Start date: August 2009
Phase: N/A
Study type: Interventional

Facial lacerations are a commonly encountered problem in the emergency department. Despite this, few original articles have been written concerning the management of lacerations of the lip which communicate with the oral cavity. Specifically, no study has been able to definitively show whether the use of antibiotics for these wounds decreases the infection rate. These cutaneous wounds are a unique type of laceration because they are continuously contaminated with oropharyngeal flora. Contaminated wounds result in larger, less cosmetic scars. Scars which involve the face have been shown to have a negative psychological impact. In this study, the investigators aim to determine whether the use of antibiotics decrease the rate of infection in lacerations of the lip which communicate with the oral cavity. Patients will be randomized to one of two currently practiced therapies. Patients will receive either cephalexin or no treatment following the repair of their through-and-through lip lacerations to determine whether antibiotics decrease the infection rate in these wounds.

NCT ID: NCT00955474 Terminated - Clinical trials for Major Depressive Disorder With Psychotic Features

Seroquel Alone Versus Seroquel With an SSRI for Depression With Psychotic Symptoms

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

The purpose of this study is to compare the efficacy and tolerability of Seroquel monotherapy for the treatment of Major Depression with Psychotic features with Seroquel plus Selective Serotonin Reuptake Inhibitor.