At a glance
ClinicalIndex Comparison RecordN/ACompleted· 32 enrolled
Drug / intervention
Precision Flow Plus +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.
Assessing Clinical Effect of HVNI on Patient Ambulation in Acute Care Scenarios: a Feasibility Study
In Brief
A clinical study evaluating Precision Flow Plus and Treatment as Usual for Respiratory Insufficiency and Dyspnea. Completed, enrolled 32 participants across 3 sites.
Detailed Summary
The pilot/feasibility study evaluates the ability of High Velocity Nasal Insufflation (HVNI) therapy to facilitate ambulation and mobilization in patients experiencing shortness of breath, as compared to simple oxygen therapy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRespiratory Insufficiency, Dyspnea
CountriesUnited States
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartNov 2018
Primary CompletionFeb 2019
Study CompletionMar 2019
First PostedMar 2019
TodayJul 2026
First PostedMar 22, 2019
Enrollment StartNov 21, 2018
Primary CompletionFeb 28, 2019
Study CompletionMar 11, 2019
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 7.3 years ago
Interventions
Precision Flow Plusdevice
High velocity nasal insufflation
Treatment as Usualdevice
Conventional therapy per institution