CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 47 enrolled
Drug / intervention
High-flow humidified nasal oxygen delivery system +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01925534
NCT01925534N/ACompleted

Pilot Study of Optiflow as a NIV Rest Therapy

Tufts Medical Center·interventional·Posted Aug 19, 2013·Updated Jul 3, 2024

In Brief

A clinical study evaluating High-flow humidified nasal oxygen delivery system and Standard oxygen therapy for Acute Respiratory Failure and Treatment With Noninvasive Positive Pressure Ventilation. Completed, enrolled 47 participants across 2 sites.

Detailed Summary

The purpose of this study is to assess whether Optiflow, a high-flow humidified oxygen delivery system, is superior to standard oxygen therapy during breaks off noninvasive ventilation in patients affected by acute respiratory failure and in respiratory distress. The investigators anticipate that the Optiflow will provide oxygen more effectively, be more comfortable and permit longer breaks off NIV, shortening the total duration of NIV.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedAug 19, 2013
Enrollment StartNov 1, 2013
Primary CompletionMay 1, 2015
Study CompletionDec 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 12.9 years ago

Interventions

High-flow humidified nasal oxygen delivery systemdevice

During breaks from NIV oxygen will be provided through the Optiflow with FiO2 and flow-rate titrated to maintain the oxygen saturation (SpO2) above 90%.

Standard oxygen therapydevice

During breaks from NIV oxygen will be provided by standard nasal cannula or mask to maintain the SpO2 above 90%.