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NCT00880906 · ClinicalTrials.gov registry record · NA

Study of the Efficiency of Esophageal Dilation on Patient With Eosinophilic Esophagitis

A NA study, sponsored by Vanderbilt University.

Completed
Registry status
NA
Development phase
50
Enrollment target

NCT00880906: Completed NA study, sponsored by Vanderbilt University.

NCT00880906 is a NA study that has completed, run by Vanderbilt University. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00880906, a NA study, has completed, sponsored by Vanderbilt University.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

This study is for patients who have had a food impaction and/or difficulty swallowing, who are scheduled to have endoscopy, biopsy and possibly dilatation (stretching) of the esophagus. Standard treatment for people who have food impaction and difficulty swallowing is endoscopy to view the esophagus, tissue biopsies of the lining of the esophagus for diagnosis, and drug therapy including steroids and drugs used to treat reflux disease. Early dilatation or stretching of the esophagus may be done at this time but not always. Some doctors prefer to wait and see if the drugs are affective. It is not known if dilating the esophagus early in treatment adds benefit. Therefore, we are doing this study to compare the two methods of treatment. We will compare two groups: one group will have dilatation performed during the first endoscopy and one group will not have dilatation performed during endoscopy. We will see if dilatation helps prevent food impaction and improves swallowing. Another purpose of this study is to learn more about the causes of swallowing problems, thus extra biopsies will be taken of the esophagus and store them for future research.

Primary Outcome

Dysphagia Scores: 0 = able to eat normal diet / no dysphagia. 1. = able to swallow some solid foods 2. = able to swallow only semi solid foods 3. = able to swallow liquids only 4. = unable to swallow anything / total dysphagia

Interventions

  • PROCEDURE Esophageal dilation
  • DRUG Steroid and Proton Pump Inhibitor Therapy

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2008-08
Est. Completion 2013-12
Phase NA
Vanderbilt University

430 total trials

What the finished NCT00880906 record still lists

NCT00880906 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Esophageal dilation is the first listed.

NCT00880906 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00880906 about?

NCT00880906 is a clinical study titled "Study of the Efficiency of Esophageal Dilation on Patient With Eosinophilic Esophagitis". This study is for patients who have had a food impaction and/or difficulty swallowing, who are scheduled to have endoscopy, biopsy and possibly dilatation (stretching) of the esophagus. Standard treatment for people who have food impaction and difficulty swallowing is endoscopy to view the esophagu...

What is the current status of trial NCT00880906?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2008-08. Estimated completion is 2013-12.

What interventions are being tested in trial NCT00880906?

The interventions under investigation include: Esophageal dilation (PROCEDURE), Steroid and Proton Pump Inhibitor Therapy (DRUG).

Who is sponsoring clinical trial NCT00880906?

This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00880906's enrollment target sits among peer trials

50 1279th of 2000 higher than 622 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00880906, the US trial registry maintained by the National Library of Medicine. NCT00880906 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.