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Inflammation clinical trials

View clinical trials related to Inflammation.

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NCT ID: NCT00878033 Completed - Clinical trials for Chronic Renal Failure

Autonomic Dysfunction and Inflammation in Chronic Hemodialysis Patients

Start date: April 2009
Phase: N/A
Study type: Observational

This study investigates the relationship between autonomic dysfunction and chronic inflammation in hemodialysis patients.

NCT ID: NCT00871234 Completed - HIV Infections Clinical Trials

Effects of Etravirine on Endothelial Function in HIV-uninfected Adults: A Pilot Study

Start date: April 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and effects of etravirine, an HIV antiretroviral medication, on vascular function.

NCT ID: NCT00869596 Completed - Airway Inflammation Clinical Trials

Study of Biomarkers of Airway Inflammation (0000-128)

Start date: March 2009
Phase: Phase 1
Study type: Interventional

This study will evaluate the effects of inhaled fluticasone on cell counts and inflammatory mediators measured in sputum of healthy volunteers following exposure to inhaled lipopolysaccharide.

NCT ID: NCT00866450 Completed - Clinical trials for Colorectal Inflammation

Effects of a Western-type Diet on Colorectal Inflammation

Start date: February 2009
Phase: Phase 0
Study type: Interventional

This study will look at the inflammatory (changes usually associated with infection/injury to the body) and bowel permeability (bowel's ability to allow contents to enter the body) effects of a Western-style diet (high fat and low in calcium) and a prudent-style diet (low fat and high in calcium) on the colon (large bowel). This study may provide information to prevent colorectal cancer in a high-risk population

NCT ID: NCT00863564 Completed - Obesity Clinical Trials

Acute Effects of Dietary Proteins on Postprandial Lipemia, Incretin Responses and Subclinical Inflammation in Obese Subjects

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

The purpose of this study is to determine the effects of dietary protein on blood lipids and gut hormones after a fat-rich meal. Hypothesis: Certain dietary proteins reduce the amount of fat circulating in the blood stream following a fat rich meal. The effect is dependant of both the quality and the quantity of protein ingested.

NCT ID: NCT00860197 Completed - Clinical trials for Low-grade Inflammation

Immune Benefits of Coffee

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

This study will assess whether coffee consumption: - increases immune responses - decreases inflammatory status

NCT ID: NCT00858195 Completed - Inflammation Clinical Trials

A Relative Bioavailability Study of 75mg Indomethacin Extended-Release Capsules

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

The purpose of this study is to demonstrate the bioequivalence of Indomethacin ER Capsules.

NCT ID: NCT00857038 Not yet recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Doxycycline and Airway Inflammation in Chronic Obstructive Pulmonary Disease (COPD)

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

COPD is a progressive pulmonary disease that is characterized by an inflammatory process in the airways and the lungs which leads to progressive airway obstruction. The inflammation is associated with tissue loss and remodelling. The investigators hypothesized that doxycycline reduces neutrophilic airway inflammation in patients with COPD. Therefore the investigators will conduct a randomized trial of doxycycline in 30 patients.

NCT ID: NCT00853970 Completed - Pain Clinical Trials

Efficacy Study of Bromfenac Ophthalmic Solution in Patients Undergoing Cataract Surgery

Start date: February 2009
Phase: Phase 3
Study type: Interventional

Efficacy study of Bromfenac Ophthalmic Solution in cataract surgery

NCT ID: NCT00852943 Active, not recruiting - Immune Deficiency Clinical Trials

Screening Protocol for Genetic Diseases of Allergic Inflammation

Start date: November 2, 2010
Phase:
Study type: Observational

Background: - Mast cells are responsible for most symptoms of allergic reactions. In some allergic diseases, it is unusually easy to cause mast cells to release their contents and cause allergic reactions. In other cases, mast cells grow abnormally and, in rare cases, can result in tumors. Mast cells also control other parts of the immune system. - Understanding why mast cells behave abnormally in allergic diseases is important to finding better ways for diagnosing and treating these potentially life-threatening disorders. Objectives: - To screen mast cells at the genetic and functional levels to characterize abnormalities, identify mutations, detect carrier states, and/or develop therapies for such disorders. - To create a library of information about inherited diseases of mast cell homeostasis and activation, including piebaldism (problems with skin and hair pigmentation), anaphylaxis (severe allergic reaction), allergies, asthma, atopic dermatitis (eczema), allergic rhinitis ( hay fever ), food allergies, urticaria/angioedema (hives/swelling), immunodeficiency diseases, and autoimmune diseases. Eligibility: - Patients between the ages of 1 and 80 years who have been referred by a physician and are known to have or be suspected of having an inherited disorder of mast cells, in particular patients (and their relatives) with piebaldism, allergies, or anaphylaxis that is not caused by allergies. Design: - Study population will consist of up to 1000 participants in a 5-year period. One third of the study population will consist of patients; the other two thirds will consist of biological relatives. - Evaluation is limited to testing on blood specimens; no treatment will be provided. - Clinical and research laboratory evaluations of patients will include the following: - Clinical evaluation and previous laboratory tests as documented in outside medical records by health care providers. A standard questionnaire will also be administered at the time of subject enrollment. - Blood collection for clinical laboratory testing, tailored to each subject s clinical evaluation where appropriate (5 ml). - Blood collection for research laboratory testing, tailored to each subject s clinical evaluation including genetic screening and assessment of mast cell growth and functioning and storage of additional frozen blood specimens for future studies (up to an additional 30 ml). - Evaluations of blood relatives will include the following: - Clinical evaluation as documented from outside medical records by health care providers and administration of a standard questionnaire. - Blood collection where indicated for diagnostic or research purposes. - After 12 consecutive months on the study, results from initial evaluation will be reviewed. Subjects with findings deemed to be of continued interest will be contacted and invited to remain as active participants to this protocol for another year, provided that they renew their consent to participate.