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NCT00880594 · ClinicalTrials.gov registry record · NA

Irritable Bowel Syndrome (IBS) Functional Magnetic Resonance Imaging (fMRI) With Desipramine

A NA study, sponsored by Washington University School of Medicine.

Terminated
Registry status
NA
Development phase
18
Enrollment target

NCT00880594 is a NA study that was terminated before completion, run by Washington University School of Medicine. The registered enrollment target is 18 participants.

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The verdict

NCT00880594, a NA study, was terminated before completion, sponsored by Washington University School of Medicine.

TERMINATED
Registry status
NA
Development phase
18 participants
Enrollment target

Study Summary

Individuals with irritable bowel syndrome (IBS) may experience abdominal pain as a result of pain signals in the bowel and how these signals are processed in the brain. Studies using brain imaging (pictures) have shown that IBS patients with more pain diagnoses (i.e. fibromyalgia, migraines, etc.) have greater activity in the regions of the brain responsible for the emotional and thought processing of pain signals. This could possibly make bowel sensations and bowel difficulties feel abnormal or more noticeable, in turn causing more severe IBS symptoms. The purpose of this protocol is to explore the role of pain diagnoses and their affect on brain activity in IBS patients. The investigators will also examine the use of a medication, desipramine, which is known to affect these brain regions, in IBS patients.

Interventions

  • DRUG Desipramine

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2009-02
Est. Completion 2014-11-11
Phase NA

What the Registry Record Tells You About NCT00880594

The ClinicalTrials.gov registry entry for NCT00880594 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Desipramine is the first listed.

NCT00880594 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00880594 about?

NCT00880594 is a clinical study titled "Irritable Bowel Syndrome (IBS) Functional Magnetic Resonance Imaging (fMRI) With Desipramine". Individuals with irritable bowel syndrome (IBS) may experience abdominal pain as a result of pain signals in the bowel and how these signals are processed in the brain. Studies using brain imaging (pictures) have shown that IBS patients with more pain diagnoses (i.e. fibromyalgia, migraines, etc.) h...

What is the current status of trial NCT00880594?

This trial is currently terminated. It is a NA study. The enrollment target is 18 participants. The study started on 2009-02. Estimated completion is 2014-11-11.

What interventions are being tested in trial NCT00880594?

The interventions under investigation include: Desipramine (DRUG).

Who is sponsoring clinical trial NCT00880594?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.