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NCT01373125 · ClinicalTrials.gov registry record

Is the Neosquamous Epithelium "Normal" Following Endoscopic Ablation of Dysplastic Barrett's Esophagus?

A clinical trial of Barrett's Esophagus and Gastroesophageal Reflux Disease (GERD), sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
99
Enrollment target
1
Study location

NCT01373125 is a study of Barrett's Esophagus and Gastroesophageal Reflux Disease (GERD) that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 99 participants, below the 520-participant average among 22 other Barrett's Esophagus trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01373125, a study of Barrett's Esophagus and Gastroesophageal Reflux Disease (GERD), has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
99 participants
Enrollment target
1
Study location

Study Summary

The investigators propose a study comparing the morphological and functional aspects of the neosquamous epithelium (NSE) after ablative therapy for dysplastic Barrett's esophagus (BE) to that of native squamous epithelium in normal controls as well as gastroesophageal reflux disease (GERD), non-Barrett's Esophagus (BE) subjects.

Study Locations (1)

North Carolina

  • University of North Carolina Chapel Hill - Chapel Hill

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2011-06
Est. Completion 2014-10

What the Registry Record Tells You About NCT01373125

The ClinicalTrials.gov registry entry for NCT01373125 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 99 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 520-participant average among 22 other Barrett's Esophagus trials with a reported enrollment target (81% lower). The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Barrett's Esophagus appearing as the primary indexed condition, and to 0 interventions.

NCT01373125 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT01373125 about?

NCT01373125 is a clinical study titled "Is the Neosquamous Epithelium "Normal" Following Endoscopic Ablation of Dysplastic Barrett's Esophagus?". The investigators propose a study comparing the morphological and functional aspects of the neosquamous epithelium (NSE) after ablative therapy for dysplastic Barrett's esophagus (BE) to that of native squamous epithelium in normal controls as well as gastroesophageal reflux disease (GERD), non-Barr...

What is the current status of trial NCT01373125?

This trial is currently completed. The enrollment target is 99 participants. The study started on 2011-06. Estimated completion is 2014-10.

What conditions does trial NCT01373125 study?

This clinical trial studies the following conditions: Barrett's Esophagus, Gastroesophageal Reflux Disease (GERD), Intestinal Metaplasia.

Who is sponsoring clinical trial NCT01373125?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01373125 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.