Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Indianapolis, Indiana 46202


Purpose:

The metabolic response to ulcerative colitis, including increased proteolysis and lipolysis and changes in energy expenditure, plays a significant role in the resulting malnutrition from which these patients suffer. Tumor necrosis factor-alpha (TNF-alpha), a pro-inflammatory cytokine, has been found to be elevated in children with ulcerative colitis. TNF-alpha has been incriminated in the mechanism of weight loss in many different chronic diseases, and causes net protein and lipid catabolism. Anti-TNF-alpha antibody (infliximab) has been proven to be an effective therapy for ulcerative colitis. The purpose of this study is to determine changes in protein and lipid metabolism, as well as resting energy expenditure, before and after therapy with anti-TNF-alpha antibody (infliximab) in children with ulcerative colitis. Performing this study will better define the changes in nutrition status observed in these children following remission of active ulcerative colitis, and potentially lead to changes in medical and nutritional management of these children


Criteria:

Inclusion Criteria: - Male and female children between the ages of six and eighteen years of age - Endoscopic or histologic evidence of ulcerative colitis - Active ulcerative colitis determined by primary pediatric gastroenterologist to require anti-tumor necrosis factor-alpha antibody (infliximab) therapy - Colitis symptom score ≥2 - Screening laboratory tests that meet the following criteria (obtained within 4 weeks of enrollment): 1. Hemoglobin >8.0 g/dL 2. White blood cell count >3.5 x 109/L 3. Neutrophils >1.5 x 109/L 4. Platelets >100 x 109/L 5. Aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase levels within 3 times the upper limit of normal. 6. PPD skin test with skin induration <5 mm. 7. Signed written consent from the parent/legal guardian and assent from the child to be obtained prior to enrollment. Exclusion Criteria: - Female subjects who are pregnant, nursing, or planning pregnancy. - Concomitant diagnosis or history of congestive heart failure. - Serious infection in the 3 months prior to enrollment. - History of prior or current active or latent tuberculosis. - Immune deficiency syndrome, including documented human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS). - History of systemic lupus erythematosus. - A transplanted organ. - Known malignancy or history of malignancy within 5 years of enrollment. - History of demyelinating disease. - History of substance abuse. - History of diabetes mellitus. - Poor tolerability of venipuncture or lack of venous access during the study period. - A live virus vaccination within 3 months of enrollment. - Prior history of infliximab infusion or any other therapeutic agent targeted at reducing tumor necrosis factor-alpha (TNF-alpha). - Hypersensitivity to any murine proteins or other component of the product. - Inability to comply with study procedures


NCT ID:

NCT00586807


Primary Contact:

Principal Investigator
Steven J Steiner, MD
Indiana University


Backup Contact:

N/A


Location Contact:

Indianapolis, Indiana 46202
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 20, 2018

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.