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CompletedNCT04053751Updated May 27, 2022

Effects of Open and Closed System Suctioning on Suctioning Frequency and Amount of Secretion

An interventional study of closed suctioning system in Secretion; Excess, Salivation, sponsored by Dokuz Eylul University. Completed at 1 site in Turkey. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-05-27.

Sponsored by Dokuz Eylul University · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Tracheal suctioning is a process which is often applied to patients' care who have an artificial airway and whose respiration is achieved via mechanical ventilation. When secretions are not cleaned enough, it causes a variety of complications in the patient from hypoxemia to infection.

It is reported that the studies with nurses in clinical practice have shown that they have opinions such as the closed system does not suction the patients effectively as the open system does; it remains incapable in removing secretions, thus the suctioning process is being applied more frequently.

Therefore this study is designed to examine the amount of secretions and frequency of suctioning as a result of open and closed suctioning systems.

Read the detailed description

Patients will be monitored for two days. On the first day, the patient will be followed up with an open system and the second day closed suctioning system will be used, or the patient will be followed up with a closed system on the first day and followed with an open system on the second day. The patients are randomly allocated on the first follow up days. The follow-up period has two consecutive days. suctioning will be performed for 12 hours in one day. The number of suctions will be recorded. The amount of secretion will be accumulated in the mucus collection vessel. At the end of the day, the secretion will be weighed with precision weighing.

02

Conditions studied

  • Secretion; Excess, Salivation

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Keywords

  • intensive care unit
  • endotracheal suctioning
  • open suctioning system
  • closed suctioning system
  • nursing
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • orally intubated in first 96 hours
  • stabilized patients in conditionally
  • platelets > 50.000
  • not have hemorrhagic secretions

Exclusion criteria

Exclusion Criteria:

  • hemodynamically unstabilized patients
04

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
100 participants (actual)

Study arms

  • Experimental
    closed suctioning system

    Closed suctioning system will be compared with open suctioning system

    Procedure: closed suctioning system

  • No intervention
    open suctioning system

    The patient will be monitored with closed system for one day and open aspiration system on the other day.

Interventions

  • Procedureclosed suctioning system

    a randomized allocated patient will be monitored for two days. Closed suctioning system will evaluate as experimental group. open suctioning system will evaluate as control group.

05

What researchers measure

Primary outcomes

  1. frequency of suctioning

    frequency of suctioning in a half of a day

    Time frame: 12 hours of a day

  2. amount of secretion

    amount of secretion in a half of a day

    Time frame: 12 hours of a day

Secondary outcomes

  1. spo2

    differences in spo2 between open and closed suctioning systems

    Time frame: 12 hours of a day

  2. tidal volume

    differences in tidal volume between open and closed suctioning systems

    Time frame: 12 hours of a day

06

Study locations

1 site
  • Dokuz Eylul University
    İzmir, Turkey
07

References and documents

Individual participant data

Plan to share: No — There is no plan to share the patients data with other researchers.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT04053751
Lead sponsor
Dokuz Eylul University
Responsible party
Ilkin Yilmaz (Research Assisstant, Dokuz Eylul University) — Principal investigator
First posted
Aug 12, 2019
Start date
Aug 1, 2019
Primary completion
Dec 15, 2019
Completion
Dec 20, 2019
Last update
May 27, 2022

Study contacts

Dilek Ozden, PhD
study director · Dokuz Eylul University Faculty of Nursing
Ilkin Yilmaz, PhD
principal investigator · Dokuz Eylul University Faculty of Nursing

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2022. You cannot join it, but the record below documents what was studied.

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