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NCT02168257 · ClinicalTrials.gov registry record · NA

Neotech RAM Cannula Versus Conventional Binasal Prong Continuous Positive Airway Pressure (CPAP) to Treat Respiratory Distress in Low Birth Weight Neonates

A NA study, sponsored by Children's Hospitals and Clinics of Minnesota.

Terminated
Registry status
NA
Development phase
8
Enrollment target

NCT02168257 is a NA study that was terminated before completion, run by Children's Hospitals and Clinics of Minnesota. The registered enrollment target is 8 participants.

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The verdict

NCT02168257, a NA study, was terminated before completion, sponsored by Children's Hospitals and Clinics of Minnesota.

TERMINATED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

The purpose of this study is to determine if the RAM cannula is as effective as conventional binasal prongs to deliver CPAP to low birth weight infants with respiratory distress.

Interventions

  • DEVICE RAM Cannula
  • DEVICE Binasal Prong CPAP

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2014-06
Est. Completion 2017-02
Phase NA

What the Registry Record Tells You About NCT02168257

The ClinicalTrials.gov registry entry for NCT02168257 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Hospitals and Clinics of Minnesota, which has 31 total studies on file at ClinicalTrials.gov.

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

NCT02168257 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02168257 about?

NCT02168257 is a clinical study titled "Neotech RAM Cannula Versus Conventional Binasal Prong Continuous Positive Airway Pressure (CPAP) to Treat Respiratory Distress in Low Birth Weight Neonates". The purpose of this study is to determine if the RAM cannula is as effective as conventional binasal prongs to deliver CPAP to low birth weight infants with respiratory distress.

What is the current status of trial NCT02168257?

This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2014-06. Estimated completion is 2017-02.

What interventions are being tested in trial NCT02168257?

The interventions under investigation include: RAM Cannula (DEVICE), Binasal Prong CPAP (DEVICE).

Who is sponsoring clinical trial NCT02168257?

This trial is sponsored by Children's Hospitals and Clinics of Minnesota, which has 31 total clinical trials registered on ClinicalTrials.gov.

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

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