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Inflammation clinical trials

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NCT ID: NCT00799643 Completed - Clinical trials for Type 2 Diabetes Mellitus

Targeting Inflammation Using Salsalate for Type 2 Diabetes-Stage II

TINSALT2D-II
Start date: November 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Growing evidence over recent years supports a potential role for low grade chronic inflammation in the pathogenesis of insulin resistance and type 2 diabetes. In this study we will determine whether salsalate, a member of the commonly used Non-Steroidal Anti-Inflammatory Drug (NSAID) class, is effective in lowering sugars in patients with type 2 diabetes. The study will determine whether salicylates represent a new pharmacological option for diabetes management. The study is conducted in two stages. Enrollment in the first stage is complete. The primary objective of the first stage was to select a dose of salsalate that is both well-tolerated and demonstrates a trend toward improvement in glycemic control. The primary objective of Stage 2 of the study is to evaluate the effects of salsalate on blood sugar control in diabetes; the tolerability of salsalate use in patients with type 2 diabetes (T2D); and the effects of salsalate on measures of inflammation, the metabolic syndrome, and cardiac risk.

NCT ID: NCT00793806 Completed - Clinical trials for Chronic Kidney Disease

Immunologic Abnormalities, Chronic Inflammation and Oxidative Stress in Chronic Kidney Disease

Start date: August 2008
Phase:
Study type: Observational

The common causes of mortality are late stages of chronic kidney disease, cardiovascular disease and infections, are associated with abnormalities of the immune system, an underlying state of chronic inflammation and oxidative stress. These processes have not been carefully described in the chronic kidney disease population. The researcher can use Diffuse Optical Spectroscopy to determine the immune system in individuals with chronic kidney disease and describe the association with chronic inflammation and oxidative stress in that population.

NCT ID: NCT00791323 Completed - Inflammation Clinical Trials

Efficacy of Ketorolac 0.4% in Prostaglandin Suppression

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

A pilot study to evaluate the extent of PGE2 inhibition (mean aqueous values) by Ketorolac 0.04% following peripheral iridotomy

NCT ID: NCT00789971 Completed - Ocular Inflammation Clinical Trials

Triamcinolone Versus Topical Treatment in Post Operative Phacoemulsification

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

Cataract extraction is one of the most common operative procedures performed throughout the world. Conventionally, patients are discharged with postoperative drops of steroids and antibiotics or a combination of both. These drops are to be administered for 2-6 weeks depending on individual eye unit protocol. Many patients find the postoperative drops arduous and non-compliance can cause prolonged inflammation and discomfort. Patients with cognitive, physical and visual impairments require assistance from family or community nurses to administer drops. A single perioperative injection of Triamcinolone has been shown to be an effective replacement for drops postoperatively in two previous studies 1, 2. Aims & objectives The aim of this study is to see if a single orbital floor injection of Triamcinolone is equivalent to conventional steroid and antibiotic drops used post operatively in uneventful phacoemulsification surgery in treating postoperative inflammation.

NCT ID: NCT00785018 Completed - Inflammation Clinical Trials

In Vivo Effects of C1-esterase Inhibitor on the Innate Immune Response During Human Endotoxemia

VECTOR
Start date: November 2008
Phase: N/A
Study type: Interventional

Excessive inflammation is associated with tissue damage caused by over-activation of the innate immune system. This can range from mild disease to extreme conditions such as multiple organ failure (MOF). In marked contrast to adaptive immunity which is very sensitive to immune modulators such as steroids, the innate immune system cannot be sufficiently targeted by currently available anti-inflammatory drugs. We hypothesize that C1-esterase inhibitor can modulate the innate immune response. In this study, human endotoxemia will be used as a model for inflammation. Subjects will, additionally to endotoxin, receive C1 esterase inhibitor or placebo. Blood will be sampled to determine the levels of markers of the innate immune response.

NCT ID: NCT00780923 Completed - Inflammation Clinical Trials

Effect of Continuous Positive Airway Pressure Treatment on Inflammation in Patients With Obstructive Sleep Apnea

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

The purpose of this study is to evaluate the effects of CPAP treatment on airway and systemic inflammation in obstructive sleep apnea.

NCT ID: NCT00780520 Completed - Sepsis Clinical Trials

The Effect of Glutamine on Systemic Inflammation During Human Experimental Endotoxemia

Start date: June 2007
Phase: N/A
Study type: Interventional

Glutamine levels decrease during severe sepsis; this may be associated with increased mortality. The investigators tested the effects of glutamine supplementation on systemic inflammation in a human sepsis model. The investigators found that glutamine levels drops significantly during experimentally induced systemic inflammation. However, glutamine did not affect the degree of inflammation.

NCT ID: NCT00780481 Terminated - Obesity Clinical Trials

Characterization of Brachial Arterial t-PA Release, Endothelial Function, Obesity and Inflammation

P1A3B
Start date: January 2007
Phase: N/A
Study type: Interventional

T-PA release is impaired in obese subjects. In order to have a better mechanistic understanding of t-PA release, we will compare t-PA release to Flow Mediated Vasodilation, Radial Artery Tonometry, and other markers of endothelial function and oxidative stress.

NCT ID: NCT00776412 Completed - Inflammation Clinical Trials

Blood Markers of Inflammation, Blood Clotting and Blood Vessel Function in HIV-infected Adults

Start date: November 20, 2008
Phase:
Study type: Observational

This study will collect information about markers of inflammation, blood clotting and blood vessel function in HIV-infected adults and healthy volunteers. Biomarkers are biological indicators that have been associated with disease. Certain markers of inflammation, blood clotting, and blood vessel function have been associated with risk of cardiovascular disease, stroke and death. One marker, called D-dimer, is a breakdown product of blood clots that has been associated with serious medical conditions, including deep vein thrombosis (formation of a blood clot in a vein deep in the body) and pulmonary embolism (blockage in the pulmonary artery that occurs when a blood clot from a vein breaks away, travels to the pulmonary artery and lodges there). High D-dimer levels have also been associated with cardiovascular disease and stroke risk. In a recent study of HIV-infected patients, higher D-dimer levels were strongly correlated with risk of death from any cause. The significance of changes in D-dimer and other biomarkers in HIV-infected adults is not well understood. This study will further explore D-dimer and other biomarkers to try to better understand the relationships between them and HIV infection. Healthy volunteers and HIV-infected adults 18 years of age or older may be eligible for this study. Two visits are involved, as follows: Visit 1 (screening visit to determine eligibility) - Medical history and physical examination. - Blood tests for HIV infection, blood counts, liver and kidney function. - Pregnancy test for women who can become pregnant. Visit 2 - Blood tests for hepatitis B and C - Blood tests for markers of inflammation and blood clotting. - Blood test for genetic changes that influence blood clotting. In some cases, visits 1 and 2 may be combined. Optional additional visits (up to 8 visits over 3 years) - Additional blood draws for investigation of specific clinical or laboratory findings may be requested.

NCT ID: NCT00770497 Completed - Hypertension Clinical Trials

Efficacy Study of Pioglitazone and Ramipril Combination Therapy in Treating Non-diabetic Hypertensive Patients.

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

The purpose of this study is to determine the effects of pioglitazone, once daily (QD), on low grade inflammation and vascular function in hypertensive patients.