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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03486002
Other study ID # Pro00087066
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date July 17, 2018
Est. completion date April 17, 2020

Study information

Verified date September 2019
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to compare the effectiveness of a closed suction system with an inflatable balloon on the catheter (Cleansweep system) to that of a standard closed suction system in terms of reducing the interior resistance of endotracheal tubes. Subjects who require frequent suctioning ( > every 2.5 hours) and who have stable cardiovascular systems will be randomized to receive suctioning either through the Cleansweep system or standard system initially followed by the corresponding system. The subjects will be suctioned every two hours for eight hours ( the first 2 suction procedures with one system followed by 2 with the other system). After each suction procedure measurements of resistance will be made using peak and plateau pressures.

Analysis: For each patient, data for both procedures on each catheter system will be pooled and mean differences between the standard system and the Cleansweep system will be calculated. For all 20 patients the mean (+/- SD) of these differences will be calculated and significance will be sought using appropriate statistical tests. The study will be unblinded and randomization determines merely which system will used initially for the first 2 procedures.


Recruitment information / eligibility

Status Terminated
Enrollment 8
Est. completion date April 17, 2020
Est. primary completion date April 17, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Intubated, mechanically ventilated patients who require suctioning more often than every 2.5 hours

Exclusion Criteria:

- Unstable cardiovascular system (significant arrythmias, blood pressure support requiring > 2 pressors

- refractory hypoxemia (P/F ratio < 80)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Cleansweep
The Cleansweep closed suction system
Halyard
Halyard Closed Suction System

Locations

Country Name City State
United States Duke Health System Durham North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Duke University Teleflex

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in endotracheal tube resistance during mechanical ventilation after 4 suction procedures Measurements of resistance will be made following each suction procedure (2 with the Cleansweep system and 2 with the standard system) 8 hours