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NCT01507207 · ClinicalTrials.gov registry record · Phase 4

Pediatric Dysphagia Outcomes After Injection Laryngoplasty for Type I Laryngeal Cleft

A Phase 4 study of Quality of Life and Dysphagia, sponsored by Oregon Health and Science University.

Completed
Registry status
Phase 4
Development phase
50
Enrollment target
1
Study location

NCT01507207 is a Phase 4 study of Quality of Life and Dysphagia that has completed, run by Oregon Health and Science University. The registered enrollment target is 50 participants, below the 452-participant average among 107 other Quality of Life trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01507207, a Phase 4 study of Quality of Life and Dysphagia, has completed, sponsored by Oregon Health and Science University.

COMPLETED
Registry status
Phase 4
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

Type I laryngeal cleft evaluation and treatment in the pediatric population is an emerging science. The largest published series of pediatric patients with type I laryngeal clefts shows conflicting evidence in terms of outcomes, resolution of dysphagia and method of treatment. A comparison of quality of life outcomes before and after injection laryngoplasty has not been carried out. The investigators hypothesize that injection laryngoplasty significantly improves symptoms and quality of life related to dysphagia in a pediatric population with laryngeal clefts.

Interventions

  • PROCEDURE Injection laryngoplasty

Study Locations (1)

Oregon

  • Oregon Health & Science University - Doernbecher Children's Hospital - Portland

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2012-01
Est. Completion 2015-05-15
Phase Phase 4

What the Registry Record Tells You About NCT01507207

The ClinicalTrials.gov registry entry for NCT01507207 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 452-participant average among 107 other Quality of Life trials with a reported enrollment target (89% lower). The listed sponsor is Oregon Health and Science University, which has 546 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Quality of Life appearing as the primary indexed condition, and to 1 intervention - of which Injection laryngoplasty is the first listed.

NCT01507207 reports 1 study location spanning 1 distinct geographic area - top geographies include Oregon.

Frequently Asked Questions

What is clinical trial NCT01507207 about?

NCT01507207 is a clinical study titled "Pediatric Dysphagia Outcomes After Injection Laryngoplasty for Type I Laryngeal Cleft". Type I laryngeal cleft evaluation and treatment in the pediatric population is an emerging science. The largest published series of pediatric patients with type I laryngeal clefts shows conflicting evidence in terms of outcomes, resolution of dysphagia and method of treatment. A comparison of qualit...

What is the current status of trial NCT01507207?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2012-01. Estimated completion is 2015-05-15.

What conditions does trial NCT01507207 study?

This clinical trial studies the following conditions: Quality of Life, Dysphagia, Aspiration.

What interventions are being tested in trial NCT01507207?

The interventions under investigation include: Injection laryngoplasty (PROCEDURE).

Who is sponsoring clinical trial NCT01507207?

This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01507207 being conducted?

This trial has 1 study location across Oregon. 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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