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NCT02038894 · ClinicalTrials.gov registry record · NA

Comparing Anesthetic Techniques in Children Having Esophagogastroduodenoscopies

A NA study of Eosinophilic Esophagitis, sponsored by Children's Hospital Medical Center, Cincinnati.

Completed
Registry status
NA
Development phase
179
Enrollment target
1
Study location

NCT02038894 is a NA study of Eosinophilic Esophagitis that has completed, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 179 participants, below the 860-participant average among 44 other Eosinophilic Esophagitis trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02038894, a NA study of Eosinophilic Esophagitis, has completed, sponsored by Children's Hospital Medical Center, Cincinnati.

COMPLETED
Registry status
NA
Development phase
179 participants
Enrollment target
1
Study location

Study Summary

The purpose of this research study is to compare the safety and effectiveness of three commonly used techniques for delivering anesthesia during a procedure known as esophagogastroduodenoscopy.

Conditions Studied

Interventions

  • DRUG Propofol
  • DRUG Intubated with Sevoflurane (IS)
  • DRUG Intubated with Propofol (IP)
  • DRUG Zofran - no intubation

Study Locations (1)

Ohio

  • Cincinnati Children's Hospital Medical Center - Cincinnati

Trial Details

FieldValue
Enrollment Target 179 participants
Start Date 2009-12
Est. Completion 2013-11
Phase NA

What the Registry Record Tells You About NCT02038894

The ClinicalTrials.gov registry entry for NCT02038894 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 179 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 860-participant average among 44 other Eosinophilic Esophagitis trials with a reported enrollment target (79% lower). The listed sponsor is Children's Hospital Medical Center, Cincinnati, which has 571 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Eosinophilic Esophagitis appearing as the primary indexed condition, and to 4 interventions - of which Propofol is the first listed.

NCT02038894 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT02038894 about?

NCT02038894 is a clinical study titled "Comparing Anesthetic Techniques in Children Having Esophagogastroduodenoscopies". The purpose of this research study is to compare the safety and effectiveness of three commonly used techniques for delivering anesthesia during a procedure known as esophagogastroduodenoscopy.

What is the current status of trial NCT02038894?

This trial is currently completed. It is a NA study. The enrollment target is 179 participants. The study started on 2009-12. Estimated completion is 2013-11.

What conditions does trial NCT02038894 study?

This clinical trial studies the following conditions: Eosinophilic Esophagitis.

What interventions are being tested in trial NCT02038894?

The interventions under investigation include: Propofol (DRUG), Intubated with Sevoflurane (IS) (DRUG), Intubated with Propofol (IP) (DRUG), Zofran - no intubation (DRUG).

Who is sponsoring clinical trial NCT02038894?

This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02038894 being conducted?

This trial has 1 study location across Ohio. 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

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