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Inflammation clinical trials

View clinical trials related to Inflammation.

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NCT ID: NCT01607619 Completed - Inflammation Clinical Trials

Effect of Anatabine on Elevated Blood Levels of C-reactive Protein

Start date: May 2011
Phase: N/A
Study type: Interventional

The investigators are studying a dietary supplement called anatabine in a lozenge form named RCP006. The main purpose of this study is to evaluate the effects of this dietary supplement on normal human inflammatory function. The investigators will see this effect in volunteers who have markers of higher levels of inflammation to begin with. The investigators anticipate that anatabine will reduce markers of inflammation. Therefore the investigators are looking for volunteers with high blood levels of C-reactive Protein (CRP) and will monitor the blood CRP levels at several time points throughout the study.

NCT ID: NCT01606735 Completed - Clinical trials for Inflammation Associated With Cataract Surgery

Efficacy and Safety of IBI-10090 in Ocular Surgery Patients

Start date: April 2012
Phase: Phase 2
Study type: Interventional

This study will test the efficacy and safety of IBI-10090 in the treatment of ocular inflammation after ocular surgery.

NCT ID: NCT01604213 Completed - Clinical trials for Type 2 Diabetes Mellitus

Effects of Vildagliptin/Metformin Combination on Markers of Atherosclerosis, Thrombosis, and Inflammation in Diabetics With Coronary Artery Disease

VAAST
Start date: September 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to demonstrate that combined vildagliptin-metformin therapy is associated with clinically significant reductions in biological markers of inflammation, pro-thrombogenicity, and atherosclerosis as compared to metformin mono-therapy in a population of diabetic patients with coronary artery disease who undergo cardiac rehabilitation. The pre-specified established biological markers of inflammation, pro-thrombogenicity, and atherosclerosis will include: interleukin-6 (IL-6 - primary biological marker), hs-CRP, platelet reactivity testing, MMP-9, Interleukin 1 beta (IL-1 beta) and adiponectin levels.

NCT ID: NCT01603030 Not yet recruiting - Clinical trials for Eye Infection/Inflammation Other

Efficacy of Moxifloxacin/Prednisolone in Prevention of Post Surgery Inflammation

Start date: June 2012
Phase: Phase 3
Study type: Interventional

This is a Unicentric, double-blind, randomized, two-arm, parallel-group study to demonstrate the efficacy of moxifloxacin/prednisolone acetate fixed combination compared with individual administration of moxifloxacin + acetate Prednisolone Eye drops in Prevention of Post Operative Inflammation and Infection in LASIK surgery.

NCT ID: NCT01601821 Completed - Inflammation Clinical Trials

Open Label Comparative Study Of De Novo Renal Allograft Recipients Receiving CSA + MMF + Corticosteroids Versus CSA + Rapamune + Corticosteroids

Start date: April 2006
Phase: Phase 4
Study type: Interventional

To compare the safety and efficacy of cyclosporine (CsA) + mycophenolate mofetil (MMF) + corticosteroids © to CsA + Rapamune + Cs with CsA elimination in the Rapamune arm with the introduction of MMF in de novo renal allograft recipients.

NCT ID: NCT01601106 Recruiting - Inflammation Clinical Trials

Silencing Inflammatory Activity by Injecting Nanocort in Patients at Risk for Atherosclerotic Disease

SILENCE
Start date: September 2011
Phase: Phase 1/Phase 2
Study type: Interventional

Cardiovascular disease(CVD) is the leading cause of morbidity and mortality in developed nations. CVD is primarily caused by atherosclerosis, a systemic disease characterized by lipid deposition in the subendothelial space with a concomitant, low-grade inflammatory reaction.(Fuster, Moreno et al. 2005) To date, most therapeutic interventions aimed at lowering CVD have thus far focused on modulating lipid levels, either lowering LDLc or increasing HDLc levels. Yet, since the introduction of statins 20 years ago, there have been few breakthroughs in the treatment of this disease. A promising strategy to reduce CVD is to directly target inflammation at the level of the vessel wall.(van Leuven, van Wijk et al.; Libby 2002) A potential drawback of anti-inflammatory strategies pertains to the thin line between inhibiting 'inappropriate' inflammation versus inducing immuno-suppression. Therefore, continuous low dosed anti-inflammatory drugs have great potential as novel treatment strategies. In the present project, the investigators propose to inject liposomal glucocorticoids intravenously in patients with an increased risk of atherosclerotic disease aiming to reduce vessel wall inflammation.

NCT ID: NCT01594008 Completed - Inflammation Clinical Trials

The Effects of Antioxidants in Blueberry Powder on Inflammation Induced by a Single High Fat Meal.

FL89
Start date: January 2012
Phase: N/A
Study type: Interventional

The goal of the study is to find out whether a high fat meal increases blood lipids and causes monocyte (white blood cell) activation, and whether blueberry intake at the same meal lessens monocyte activation in healthy people.

NCT ID: NCT01593124 Completed - Vaginal Infections Clinical Trials

Identification of Novel Biomarkers of Cervicovaginal Mucosal Inflammation

Biomarkers
Start date: May 2012
Phase: Phase 2
Study type: Interventional

This study investigates the response of vaginal and cervical tissue after exposure to three vaginal products: hydroxyethyl cellulose (HEC) placebo, nonoxynol-9 (N9) and imiquimod (IMQ) cream.

NCT ID: NCT01591655 Completed - Surgery Clinical Trials

Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

Start date: July 2012
Phase: Phase 3
Study type: Interventional

The objective of this clinical study is to compare the safety and efficacy of mapracorat ophthalmic suspension, 3% with its vehicle for the treatment of postoperative inflammation and pain following cataract surgery. Participants from the United States and Canada will be recruited for this study.

NCT ID: NCT01591161 Completed - Surgery Clinical Trials

Mapracorat Ophthalmic Suspension, 3% for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

Start date: July 2012
Phase: Phase 3
Study type: Interventional

The objective of this clinical study is to compare the safety and efficacy of mapracorat ophthalmic suspension, 3% with its vehicle for the treatment of postoperative inflammation and pain following cataract surgery.