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NCT00340444 · ClinicalTrials.gov registry record

Genetic Studies of Inflammatory Bowel Disease

A clinical trial, sponsored by National Human Genome Research Institute (NHGRI).

Completed
Registry status
10,000
Enrollment target

NCT00340444: Completed study, sponsored by National Human Genome Research Institute (NHGRI).

NCT00340444 is a clinical trial that has completed, run by National Human Genome Research Institute (NHGRI). The registered enrollment target is 10,000 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00340444 has completed, sponsored by National Human Genome Research Institute (NHGRI).

COMPLETED
Registry status
10,000 participants
Enrollment target

Study Summary

This study will examine the existence of genetic regions that are believed to bring about a risk for inflammatory bowel disease (IBD), with its subtypes of Crohn's disease and ulcerative colitis. It will identify the locations of chromosomes responsible for hereditary IBD through linkage analysis, a technique in genetic research in which the occurrence of a disorder in a family is evaluated alongside a known genetic disorder. The project will also do fine mapping of genes and examine possible genes associated with IBD. IBD is a chronic and often disabling disorder of the gastrointestinal tract, affecting about 500,000 Americans. Both Crohn's disease and ulcerative colitis share many characteristics, such as abdominal pain, bloody diarrhea, fever, fatigue, and malnutrition. But the main factors that distinguish these subtypes depend on the location and depth of inflammation. Tests and analyses can generally pinpoint some of the differences between the two, but sometimes there are major overlaps in characteristics, and the diagnosis is known as indeterminate IBD. The exact cause of IBD is not known, but genetic and environmental factors are known to contribute to risk for the disease. The single most important environmental risk factor has been smoking exposure at the time the diagnosis is made. Also, several genetic risk factors are ethnicity, family history, and polymorphisms-abilities to take on different forms-in the NOD2 gene. Patients who have a diagnosis of IBD and their family members 5 years of age and older who have or do not have that diagnosis may be eligible for this study. Participants will be asked to complete a questionnaire on their health, ethnic background, religion, habits, family medical history, and medications. Information will also be sought on the diagnosis, course, complications, and treatment of IBD, as well as risk factors. In addition, there will be collection of blood to be used for DNA preparation, storage of lymphocytes, and informat

Trial Details

FieldValue
Enrollment Target 10,000 participants
Start Date 2003-11-06
Est. Completion 2007-09-19

What the finished NCT00340444 record still lists

NCT00340444 is an observational study that tracks outcomes without assigning an intervention. Its 10,000 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 0 interventions.

NCT00340444 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00340444 about?

NCT00340444 is a clinical study titled "Genetic Studies of Inflammatory Bowel Disease". This study will examine the existence of genetic regions that are believed to bring about a risk for inflammatory bowel disease (IBD), with its subtypes of Crohn's disease and ulcerative colitis. It will identify the locations of chromosomes responsible for hereditary IBD through linkage analysis, a...

What is the current status of trial NCT00340444?

This trial is currently completed. The enrollment target is 10,000 participants. The study started on 2003-11-06. Estimated completion is 2007-09-19.

Who is sponsoring clinical trial NCT00340444?

This trial is sponsored by National Human Genome Research Institute (NHGRI), which has 185 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00340444, the US trial registry maintained by the National Library of Medicine. NCT00340444 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.