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Inflammation clinical trials

View clinical trials related to Inflammation.

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NCT ID: NCT00455377 Completed - Airway Inflammation Clinical Trials

Lung Function and Airway Inflammation in Portland Cement Workers

SPUTUM
Start date: March 2007
Phase: N/A
Study type: Observational

The aim of the study is to examine inflammation in the airways and in peripheral blood, in workers in a cement plant i Norway.

NCT ID: NCT00449410 Completed - Atrial Fibrillation Clinical Trials

Silent Cerebrovascular Lesion and Cognitive Decline Prevention by Cholesterol Lowering in Elderly AF Patients

SPACE
Start date: May 2005
Phase: Phase 4
Study type: Interventional

In elderly patients with atrial fibrillation (AF) the presence of silent brain infarcts and neurocognitive deficit is high despite adequate treatment with oral anticoagulation. Atherosclerosis is considered to be a chronic inflammatory disease and thrombosis and inflammation are strongly correlated. Atrial fibrillation is linked with increased levels of inflammatory markers and intensive cholesterol lowering has proven to reduce inflammation. In a prospective double-blind randomized pilot-study we want to test the hypothesis, that addition of intensive cholesterol lowering treatment besides adequate oral anticoagulation will reduce cerebrovascular lesions and will be beneficial for neurocognitive status in elderly AF patients.

NCT ID: NCT00444717 Completed - Metabolic Syndrome Clinical Trials

Impact of Pitavastatin in Hypercholesterolemic Patients With Metabolic Syndrome

Start date: April 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate anti-oxidative and anti-inflammatory effects of pitavastatin in hypercholesterolemic patients with the metabolic syndrome.

NCT ID: NCT00441844 Completed - Type 1 Diabetes Clinical Trials

Monocyte Function and Inflammation in Type 1 Diabetes and Its Modulation

Start date: October 2002
Phase: Phase 2
Study type: Interventional

Type I diabetes (T1DM) is associated with an increased risk of vascular complications. While the precise mechanism(s) by which diabetes accelerates atherosclerosis has not been elucidated, several lines of evidence point to the role of increased inflammation in the pathogenesis of these vasculopathies. The monocyte-macrophage is a pivotal cell in atherogenesis and is readily accessible for study. However, there is scanty data on monocyte function and inflammation in T1DM. Simvastatin, a HMG-CoA reductase inhibitor, has recently been shown to reduce cardiovascular events in diabetic patients (T1DM and T2DM in the Heart Protection Study). Recent studies demonstrate that simvastatin decreased C-reactive protein and decreased pro-atherogenic activity of monocytes in non-diabetic subjects. However, there is a paucity of data on the effect of simvastatin on inflammation and monocyte function in Type 1 diabetes. Thus, the purpose of this study is Aim 1) to assess biomarkers of inflammation in T1DM compared to matched controls (n=50/group). Aim 2) Also, we will assess the effect of simvastatin (20mg/day) therapy on inflammation and monocyte function in T1DM in a randomized, placebo-controlled, double blind trial.

NCT ID: NCT00440908 Completed - Inflammation Clinical Trials

Inflammation and Nutritional Parameters in Hemodialysis Patients Using Reprocessed Dialyzers

Start date: March 2007
Phase: N/A
Study type: Observational

The study is a prospective cohort trial utilizing sequential laboratory results from excess serum obtained from hemodialysis patients (acting as their own controls). The objective of this study is to determine the impact of converting from reuse to single use of dialyzers on specific markers of nutrition (pre-albumin) and inflammation (CRP) in hemodialysis patients followed over a period of 6-months after conversion. The Hypothesis is: Comparing values obtained at baseline to values at the end of 6-months after conversion from reuse to single use in the same patients: 1. In patients with baseline CRP > 5 mg/L: Mean decrease of 5 mg/L 2. In patients with baseline CRP < 5 mg/L: > 95% will remain < 5 mg/L 3. Mean serum pre-albumin levels will increase by at least 3 mg/dL. The study population will be drawn from ~2,900 patients that are currently undergoing hemodialysis in 48 dialysis units that have been identified as continuing to reuse dialyzers and specifically are using a peracetic acid-based disinfectant (Renalin®), as of February 1, 2007. These facilities will be scheduled to convert to single use of dialyzers between May and December, 2007. The selection of patients will depend solely on the facility conversion date, on a first-come, first-served basis. All patients within the dialysis facility that provide blood specimen for their routine monthly lab draws will be eligible. The facilities and patients will be enrolled consecutively until the desired sample size of approximately 2,500 patients is reached

NCT ID: NCT00439881 Completed - Inflammation Clinical Trials

A Study To Look At The Safety Of SB-681323 In Healthy Adult Subjects After Intravenous Administration Of A Single Dose

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

SB-681323 inhibits the action of an enzyme which is known to contribute to the inflammation seen in such conditions as Chronic Obstructive Pulmonary Disease and Rheumatoid Arthritis. This study will explore the safety of this drug and its blood levels when given in intravenous form to healthy human volunteers.

NCT ID: NCT00431028 Terminated - Inflammation Clinical Trials

Sub-Tenon's Injection of Triamcinolone and Ciprofloxacin in a Controlled-Release System for Cataract Surgery

Start date: September 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to compare one intraoperative sub-Tenon's capsule injection of triamcinolone and ciprofloxacin in a biodegradable controlled-release system with conventional prednisolone and ciprofloxacin eye drops to treat ocular inflammation and for infection prophylaxis after cataract surgery.

NCT ID: NCT00430092 Completed - Inflammation Clinical Trials

Study of Difluprednate in the Treatment of Inflammation Following Ocular Surgery (ST-601A-002b)

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

The purpose of this phase III study is to determine the efficacy of difluprednate in the treatment of inflammation following ocular surgery.

NCT ID: NCT00429923 Completed - Inflammation Clinical Trials

Study of Difluprednate in the Treatment of Inflammation Following Ocular Surgery (ST-601A-002a)

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

The purpose of this phase III study is to determine the efficacy of difluprednate in the treatment of inflammation following ocular surgery.

NCT ID: NCT00428246 Completed - Hypertension Clinical Trials

Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its Protective Effect on Inflammation

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

The study is about possible protective effects of paricalcitol (Zemplar) upon inflammation, blood pressure and kidney function. Kidney Inflammation occurs when white blood cells become abnormally stimulated and accumulate in the kidney and cause damage to the kidney. The purpose of this study is to determine if paricalcitol helps improve kidney injury, blood pressure control and kidney function in patients with chronic kidney disease. The study will last about 7 weeks and involves about 8 visits to the medical center.