CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 272 enrolled
Drug / intervention
CleanSweep Closed Suction Systemdevice
Likely dose
CleanSweep Closed Suction System with balloon sweeping technologyAI-extracted
Key inclusion· 2
  • Orally intubated patient with endotracheal tube
  • Mechanically ventilated less than 24 hours prior to enrollment
Key exclusion· 4
  • Less than 18 years old
  • Tracheostomy tube
  • Extracorporeal membrane oxygenation
  • Transfer from outside hospital with more than 24 hours of mechanical ventilation

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

Search/NCT03868735
NCT03868735N/ACompleted

Evaluation of the CleanSweep™ Closed Suction System on Length of Mechanical Ventilation and Ventilator-Associated Events

Rush University Medical Center·interventional·Posted Mar 11, 2019·Updated Mar 23, 2023

In Brief

A clinical study evaluating CleanSweep Closed Suction System for Mechanical Ventilation Complication. Completed, enrolled 272 participants across 1 site.

Detailed Summary

The primary aim of this study is to evaluate the CleanSweep™ Closed Suction System on time to first successful spontaneous breathing trial in mechanically ventilated patients in the medical intensive care unit. Secondary aims of this study are to evaluate the use endotracheal tube sweeping compared to closed suctioning effect on length of mechanical ventilation, length of ICU stay, length of total hospital stay, and occurrence of ventilator-associated events.

Study Details

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

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedMar 11, 2019
Enrollment StartOct 28, 2019
Primary CompletionMay 1, 2022
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 7.3 years ago

Interventions

CleanSweep Closed Suction Systemdevice

Device with balloon sweeping technology