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NCT03346343 · ClinicalTrials.gov registry record · NA

Pulmonary Function Using Non-invasive Forced Oscillometry

A NA study of Bronchopulmonary Dysplasia and Respiratory Distress Syndrome, Newborn, sponsored by University of Alabama at Birmingham.

Active
Registry status
NA
Development phase
600
Enrollment target
1
Study location

NCT03346343 is a NA study of Bronchopulmonary Dysplasia and Respiratory Distress Syndrome, Newborn that is active but no longer recruiting, run by University of Alabama at Birmingham. The registered enrollment target is 600 participants, above the 216-participant average among 29 other Bronchopulmonary Dysplasia trials with a reported enrollment target (178% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT03346343, a NA study of Bronchopulmonary Dysplasia and Respiratory Distress Syndrome, Newborn, is active but no longer recruiting, sponsored by University of Alabama at Birmingham.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
600 participants
Enrollment target
1
Study location

Study Summary

The purpose of this observational study is to measure pulmonary function in term and preterm infants with and without pulmonary disease including respiratory distress syndrome, bronchopulmonary dysplasia, transient tachypnea of the newborn, meconium aspiration syndrome, and response to treatments given to newborn infants with lung diseases using a non-invasive airway oscillometry system.

Interventions

  • DEVICE Non-invasive forced airway oscillometry

Study Locations (1)

Alabama

  • University of Alabama at Birmingham - Birmingham

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2017-12-06
Est. Completion 2027-05
Phase NA

Sponsor

University of Alabama at Birmingham

1,160 total trials

What the Registry Record Tells You About NCT03346343

The ClinicalTrials.gov registry entry for NCT03346343 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 216-participant average among 29 other Bronchopulmonary Dysplasia trials with a reported enrollment target (178% higher). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.

The record links to 6 conditions, with Bronchopulmonary Dysplasia appearing as the primary indexed condition, and to 1 intervention - of which Non-invasive forced airway oscillometry is the first listed.

NCT03346343 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.

Frequently Asked Questions

What is clinical trial NCT03346343 about?

NCT03346343 is a clinical study titled "Pulmonary Function Using Non-invasive Forced Oscillometry". The purpose of this observational study is to measure pulmonary function in term and preterm infants with and without pulmonary disease including respiratory distress syndrome, bronchopulmonary dysplasia, transient tachypnea of the newborn, meconium aspiration syndrome, and response to treatments gi...

What is the current status of trial NCT03346343?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 600 participants. The study started on 2017-12-06. Estimated completion is 2027-05.

What conditions does trial NCT03346343 study?

This clinical trial studies the following conditions: Bronchopulmonary Dysplasia, Respiratory Distress Syndrome, Newborn, Infant, Newborn, Diseases, Infant, Premature, Diseases, Transient Tachypnea of the Newborn.

What interventions are being tested in trial NCT03346343?

The interventions under investigation include: Non-invasive forced airway oscillometry (DEVICE).

Who is sponsoring clinical trial NCT03346343?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03346343 being conducted?

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

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