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Intestinal Diseases clinical trials

View clinical trials related to Intestinal Diseases.

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NCT ID: NCT00640809 Completed - Clinical trials for Bowel Diseases, Inflammatory

Comparison of Small Bowel Lesions Associated With Celecoxib Versus Ibuprofen Plus Omeprazole

Start date: October 2003
Phase: Phase 4
Study type: Interventional

To evaluate the small bowel lesion pattern associated with celecoxib alone versus ibuprofen plus omeprazole

NCT ID: NCT00639821 Completed - Clinical trials for Inflammatory Bowel Diseases

Mucosal Gene Expression Defects in IBD

Start date: July 2004
Phase: N/A
Study type: Observational

This study investigated the mucosal gene expression defects associated with active Crohn's disease (CD)and ulcerative colitis (UC), and studied the effect of infliximab induced downregulation of inflammation and mucosal healing on these abnormalities, using whole genome gene expression microarrays.

NCT ID: NCT00628823 Completed - Celiac Disease Clinical Trials

Treatment of Mild Enteropathy Celiac Disease

TMCD
Start date: March 2003
Phase: N/A
Study type: Interventional

The main purpose of this study is to evaluate the natural history of gluten sensitivity in endomysial antibody positive adults with celiac disease suspicion, who were found to have a only mild enteropathy (Marsh I-II) in the small-bowel mucosa. The investigators hypothesize that these subject are indeed gluten-sensitive, as measured by clinical, serological and histological indicators. If this would be the case, the current diagnostic criteria for celiac disease might need re-evaluation.

NCT ID: NCT00620126 Completed - Ulcerative Colitis Clinical Trials

The Home Telemanagement (UC HAT) Trial for Patients With Ulcerative Colitis

UCHAT
Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if home automated telemanagement improves bowel symptoms, quality of life, compliance with medications, and health care utilization compared to best available care in patients with ulcerative colitis.

NCT ID: NCT00620061 Completed - Clinical trials for Opioid-Induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction: Long-Term Assessment of Lubiprostone

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the long-term safety and efficacy of lubiprostone administration in participants with opioid-induced bowel dysfunction.

NCT ID: NCT00617396 Completed - Clinical trials for Functional Bowel Disorders

Open Label Seroquel (Quetiapine) Study for Treatment Resistant Functional Bowel Disorder

Start date: February 2008
Phase: N/A
Study type: Interventional

Purpose: We are proposing to examine, via open label trial, the use of Seroquel® for patients with moderate to severe functional bowel symptoms who are not receiving adequate relief from their symptoms on their present regimen of SNRI or TCA antidepressant agents. Participants: Primary eligibility will be determined of patients at The UNC Center for Functional GI & Motility Disorders Clinic who score in the moderate to severe range on the Functional Bowel Disorders Severity Index (FBDSI ≥ 37) who have failed or have incomplete treatment responses of medications including at least one prior trial of antidepressant medication. Procedures (methods): We will monitor several patient and symptom related outcomes, as well as evaluate health related quality of life, psychological distress and related psychosocial measures to determine if the addition of Seroquel® over and above the use of an antidepressant improves clinical response based on an adequate relief measure as well as selected secondary outcomes. We will also determine when treatment benefit is related to effects on pain, the associated psychological co-morbidities seen in this population, or both factors.

NCT ID: NCT00597428 Completed - Clinical trials for Opioid-Induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone

OPAL
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy and safety of lubiprostone administration in patients with opioid-induced bowel dysfunction (OBD).

NCT ID: NCT00595946 Completed - Clinical trials for Opioid-Induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction: Pivotal Assessment of Lubiprostone

OPAL
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy and safety of lubiprostone administration in patients with Opioid-induced Bowel Dysfunction.

NCT ID: NCT00586352 Completed - Ulcerative Colitis Clinical Trials

Protein Metabolism in Newly Diagnosed Pediatric Inflammatory Bowel Disease

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

Inflammatory bowel disease, which includes both Crohn's disease and ulcerative colitis, is a disease of the gastrointestinal tract leading to symptoms of abdominal pain, diarrhea, and growth disturbance. Crohn's disease is a chronic inflammatory process that may affect any part of the gastrointestinal tract, whereas ulcerative colitis is typically present only in the colon. Children with inflammatory bowel disease frequently suffer from disturbances in growth, which may continue into adulthood and result in altered growth outcomes. The metabolic response to inflammatory bowel disease, including increased protein breakdown and decreased protein synthesis may play a significant role in the resulting malnutrition and growth failure from which children with inflammatory bowel disease suffer. The purpose of this study is to compare the rates of protein synthesis within the mucosal lining of the gastrointestinal tract in children Crohn's disease or ulcerative colitis to children who have normal endoscopic examinations. By comparing children with inflammatory bowel disease to normal children, we can begin to determine how alterations in protein metabolism within the lining of the gastrointestinal tract affect whole body protein metabolism, and its consequent effects on growth. In those patients diagnosed with Crohn's disease or ulcerative colitis, a follow-up study will be conducted two weeks following the initiation of steroid therapy to determine its effects on protein metabolism. We hypothesize that children with active inflammatory bowel disease will have increased rates of protein synthesis in the lining of the gastrointestinal tract than patients who have normal endoscopy, and that increases in protein breakdown and protein synthesis will be improved following steroid therapy in children with newly diagnosed inflammatory bowel disease.

NCT ID: NCT00577928 Completed - Clinical trials for Inflammatory Bowel Disease

Value of Fecal Calprotectin

Start date: April 2006
Phase: N/A
Study type: Observational

For the main goal - the accuracy of calprotectin for the diagnosis of IBD - calprotectin levels will be compared between patients with and without a diagnosis of IBD and the sensitivity, specificity and accuracy will be determined. For the secondary aim - the correlation between calprotectin levels and disease activity - in patients with IBD selected from this cohort, we will determine the association between calprotectin levels and clinical IBD score, serological markers (WBC, Hgb, Platelets, ESR, CRP, Albumin), endoscopic (disease score, pathological activity) and radiological features (bowel wall thickening, enhancement, edema, mesenteric inflammation).