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Gastrointestinal Diseases clinical trials

View clinical trials related to Gastrointestinal Diseases.

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NCT ID: NCT00741936 Completed - Constipation Clinical Trials

An Effectiveness and Safety Study of Chinese Herbal Medicine for Functional Constipation

Start date: July 2008
Phase: Phase 2
Study type: Interventional

Functional constipation (FC) is a common complaint in clinical practice, but treatment for this condition in conventional medicine is suboptimal. Complementary and alternative medicines, especially Chinese herbal medicine (CHM) are used frequently by patients, however, there is little research evidence about these commonly used CHM. The purpose of the study is evaluate the efficacy and safety of an ancient CHM formula, MaZiRenWan (MZRW), by comparing with placebo.

NCT ID: NCT00740233 Completed - Depression Clinical Trials

Web-Based Survey of Pain, Stress and Complementary and Alternative Medicine

PROCAIM
Start date: June 2008
Phase: N/A
Study type: Observational

The investigators are inviting people with fibromyalgia, IBS, interstitial cystitis, chronic pain, and other chronic and recurring conditions to sign up and participate in a year-long Internet-based survey to study the effectiveness of alternative medicine and the interactions among stress and coping, pain, and treatment outcomes. The survey is called PROCAIM, which stands for Patient-Reported Outcomes from Complementary, Alternative, and Integrative Medicine. PROCAIM was developed under a grant to UCLA researchers from the National Center for Complementary and Alternative Medicine. This is a web-based study composed of surveys that will recur at intervals over 1 year! TO ENROLL - Log in to our web site: http://www.procaim.org/ - Register as a New User. - Select clinic name: ClinicalTrials.gov. - Read and sign the Consent Form. After participants"sign" the form with their email address, participants can begin to answer the first in a series of questionnaires. The system will send participants email reminders at the time of each scheduled follow-up for one year. For further information about PROCAIM, please contact: - Deborah Ackerman, Ph.D. - Department of Epidemiology - UCLA School of Public Health - Box 951772 - Los Angeles, CA 90095-1772 - deborah.ackerman@ucla.edu

NCT ID: NCT00710359 Completed - Clinical trials for Vitamin B 12 Deficiency

Cobalamin Status in Young Children With Gastrointestinal Symptoms or Feeding Problems

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

During fetal life and infancy, an adequate cobalamin status is important for normal growth and central nervous system development. During the last years we have detected cobalamin deficiency in a number of infants admitted to the Pediatric Department with various symptoms, including neurological symptoms and feeding problems. Cobalamin treatment is given to the infants with biochemical cobalamin deficiency, and leads to loss of symptoms and in improved physical condition. In this study we want to establish the prevalence of cobalamin deficiency in infants with gastrointestinal symptoms and/or feeding problems. Cobalamin status will be investigated in all children aged 8 months and younger, admitted to the Pediatric Department with these symptoms. In a randomised intervention trial we will evaluate the effect of cobalamin supplementation in children with these symptoms and metabolic evidence of impaired cobalamin status. Study hypothesis: Cobalamin treatment given to the infants with biochemical cobalamin deficiency, will lead to loss of symptoms and in improved physical condition.

NCT ID: NCT00708253 Completed - Clinical trials for Gastrointestinal Diseases

Single- Versus Double-balloon Enteroscopy in Small Bowel Diagnostics

SBE_vs_DBE
Start date: June 2008
Phase: N/A
Study type: Interventional

Background: The small bowel has been a black box for gastrointestinal (GI) endoscopy as, until recently, most of the small bowel was not accessible with conventional endoscopes. Double-balloon enteroscopy (DBE) is an endoscopic procedure for visualizing the entire small bowel. The method was first described by Yamamoto and colleagues in 2001. Both endoscopic diagnosis and treatment can be easily performed using DBE. The first larger series, recently published, demonstrate that DBE is feasible in visualizing large parts of the small bowel. Although DBE has widely been used routinely for examining the small intestine there are a few issues which may limit its use. The preparation and handling of the DBE-endoscope is often interpreted as being complex (such as attaching the balloon to the tip of the endoscope, inflating/deflating the two balloon systems). Recently, a novel balloon enteroscope system has been developed using only a single balloon (single balloon enteroscope, SBE). SBE was designed to facilitate diagnosis and treatment of the small bowel. The endoscopist needs to manipulate only one single balloon; thereby, time and complexity for preparation of the system and for the examination itself may be reduced. However, the new SBE system may be less efficient for deep intubation of the small bowel and may cause adverse effects due to the hooking of the endoscope during straightening of the endoscope. Study Aim: The primary aim of the present study is to compare the new SBE system with the standard DBE system with respect to completeness of visualisation and insertion depth of the small bowel, as well as complications during the procedure.

NCT ID: NCT00682877 Completed - Gastroparesis Clinical Trials

A Comparison of SmartPill Capsule With Scintigraphy for Determining Gastric Residence Time - Over 65 Years Old

GETOver65
Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine the correlation between gastric residence time of the SmartPill Capsule and the time required for partial emptying of a standard radiolabeled meal as measured by gastric emptying scintigraphy for subjects 65 years of age and older.

NCT ID: NCT00677378 Completed - Esophagitis Clinical Trials

Transient Receptor Potential Vanilloid One (TRPV1) Receptor Expression in Children With Retrosternal Pain

TRPV1
Start date: December 2006
Phase: N/A
Study type: Observational

We would like to evaluate the changes in nerve innervation and TRPV1 receptor expression along with microscopic changes associated with heart burn and abdominal pain

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: 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.