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Implementation of Nasal Non-Invasive Ventilation With a RAM Cannula in the Inpatient /Outpatient Setting

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Terminated

Conditions

Chronic Respiratory Failure

Treatments

Device: Nasal non-invasive ventilation with RAM cannula

Study type

Interventional

Funder types

Other

Identifiers

NCT03473171
HSC-MS-17-0708

Details and patient eligibility

About

The purpose of this study is to implement a standardized protocol to initiate nasal non-invasive ventilation with RAM nasal cannula (NIV/RAM-NC) with Trilogy mechanical ventilator at Children Memorial Hospital inpatient and outpatient sites, as well as to explore the side effects and complications associated with the use of NIV/RAM-NC in children.

Enrollment

5 patients

Sex

All

Ages

1 day to 21 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children admitted to the Children Memorial Hermann Hospital and consulted to Pediatric Pulmonary Service for initiation of NIV/RAM-NC both at the inpatient and outpatient sites.
  • Children who fail to wean from chronic respiratory support (CPAP, BiPAP, HFNC) in whom long-term ventilation is considered between 10/2016 - 10/2017 will be included.

Exclusion criteria

  • Children with minimal setting (CPAP < 5cmH2O, HFNC < 3LPM) able to be weaned to regular nasal cannula.
  • Patients with upper airway obstruction that may be candidates for surgical procedure will be excluded.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

Nasal non-invasive ventilation with RAM cannula
Experimental group
Treatment:
Device: Nasal non-invasive ventilation with RAM cannula

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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