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

D

Dokuz Eylül University (DEU)

Status

Completed

Conditions

Secretion; Excess, Salivation

Treatments

Procedure: closed suctioning system

Study type

Interventional

Funder types

Other

Identifiers

NCT04053751
2018.KB.SAG.025

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • hemodynamically unstabilized patients

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

100 participants in 2 patient groups

closed suctioning system
Experimental group
Description:
Closed suctioning system will be compared with open suctioning system
Treatment:
Procedure: closed suctioning system
open suctioning system
No Intervention group
Description:
The patient will be monitored with closed system for one day and open aspiration system on the other day.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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