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Gastrointestinal Diseases clinical trials

View clinical trials related to Gastrointestinal Diseases.

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NCT ID: NCT00672698 Withdrawn - Clinical trials for PERIPHERAL VASCULAR DISEASES

Evaluation of Surgical Risk in Elderly Patients Submitted to Elective Surgery

Start date: November 2008
Phase: N/A
Study type: Observational

The purpose of this study is to establish the surgical risk factors and differences between different diseases in elderly patients submitted to elective surgery in our institution.

NCT ID: NCT00671177 Completed - Colonoscopy Clinical Trials

Clinical Evaluation of Water Immersion Colonoscopy Insertion Technique

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

Recent studies indicate that infusing 300 milliliters of water (in lieu of air) into the rectum and left colon through the colonoscope as it is being inserted during a colonoscopy examination can allow easier endoscope advancement. This method may prevent stretching of the colon, and ultimately reduce pain induced during colonoscopy. Improvements in patient comfort and cooperation, may increase the efficiency and success rate of complete colonoscopy. The purpose of the study is to test the efficacy of the water immersion technique in patients colonoscopy.

NCT ID: NCT00663975 Withdrawn - Cystic Fibrosis Clinical Trials

Open Label Safety Study of DCI-1020 in Pediatric Cystic Fibrosis (CF) Patients

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

Hypothesis:DCI 1020 capsules are safe and effective in treating exocrine pancreatic insufficiency in CF patients <= 2 years of age. The results of this study are intended to be submitted to the FDA as part of the NDA package for marketing approval of PANCRECARB (DCI 1020).

NCT ID: NCT00658333 Terminated - Clinical trials for Renal Transplantation

A Study Designed to Compare the Tolerability of an Increased Dose of Enteric-coated Mycophenolate Acid (MPA) in Renal Transplant Patients Whose Dose of Mycophenolate Mofetil (MMF) Was Reduced Due to Gastrointestinal Symptoms

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

To determine if conversion to enteric coated MPA allows an escalated dose of mycophenolic acid (MPA) to be tolerated in patients experiencing gastrointestinal (GI) symptoms

NCT ID: NCT00655083 Completed - Infantile Colic Clinical Trials

A Phase I Study to Evaluate the Oral Absorption of Nepadutant in Infants

Start date: March 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the gastrointestinal absorption of nepadutant after single dose as oral solution (and the effect of age on its oral absorption) in infants. Oral absorption is evaluated through the drug recovery in urine.

NCT ID: NCT00645684 Completed - Clinical trials for Gastrointestinal Diseases

Clinical Use of an Absorbable Coated Suture Material in Surgery (Safil)

Start date: April 1998
Phase: Phase 4
Study type: Interventional

The purpose is to test a coated polyglycolic acid multifilament suture in gastrointestinal surgery as part of a controlled randomized single blinded parallel group trial. The applicability and safety of the strand material used in two suture techniques (2-layer suture technique vs. 1-layer running) are to be tested on the basis of handling characteristics, the operative time consumed for the construction of the 1st anastomosis, the average time of the hospital duration for both patient groups, and the frequency of postoperative complications after discharge, 1 month and a maximum of 3-4 months. The used suture units are counted and the length of sutures determined which will be an indirect measurement of the costs of suture material for the two techniques.

NCT ID: NCT00634153 Completed - Clinical trials for Gastrointestinal Diseases

The Surgical Gastrointestinal Diseases Registry Protocol

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

By placing the medical record information of many subjects into a research registry, researchers will be able to conduct research studies directed at increasing our knowledge about Gastrointestinal Diseases.

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: NCT00612404 Completed - Clinical trials for Gastrointestinal Diseases

Symptoms and Endoscopic Results in Consideration of Pretreatment

Start date: September 2005
Phase: N/A
Study type: Observational

Under daily routine conditions and without any intervention by the sponsor regarding the selection of subjects, diagnostic procedures, therapeutic decisions (medicinal and non- medicinal therapy, dose, duration, etc.), routine assessments, the participating physicians (i.e. gastroenterologists) are asked to document relevant data in patients with gastrointestinal disorders.