Viewing Study NCT04199039



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Last Modification Date: 2024-10-26 @ 1:24 PM
Study NCT ID: NCT04199039
Status: COMPLETED
Last Update Posted: 2019-12-13
First Post: 2019-12-10

Brief Title: Effects of Endotracheal Tube Fixation Methods on Hemodynamic Parameters During Endotracheal Suction
Sponsor: Mersin University
Organization: Mersin University

Study Overview

Official Title: The Effects of Endotracheal Tube Fixation Methods on Hemodynamic Parameters During Endotracheal Suction in Cardiovascular Surgery Intensive Care Patients
Status: COMPLETED
Status Verified Date: 2019-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Background Endotracheal suction ES may cause changes like increase in blood pressure heart rate HR and decrease in peripheral oxygen saturation SpO2 which may cause changes in hemodynamic parameters HPs that increase the workload of the heart after surgery

Aim The aim of this study is to determine the effect of the methods used in endotracheal tube ET fixation on HPs systolic blood pressure SBP diastolic blood pressure DBP HR and SpO2 during ES

Study Design The sample of this prospective single-blind non-randomized clinical trial study included 86 intubated patients who were treated in the cardiovascular surgery intensive care unit CVSICU of a university hospital between September 2016 and December 2017

Methods The ET fixations of the experimental group n43 were performed with tube holders while the ET fixations of the control group n43 were performed using plasters The HPs of the patients were measured before during at the end of suction and 5 and 15 minutes after suction
Detailed Description: Information collected from the relatives of the patient patient file and the health care workers was used to fill out the Patient Information Form

When the study started the first 43 patients were assigned to the control group and the following 43 patients were assigned to the study group in the CVS ICU ET fixation in the control group was performed with plasters which are routinely used in the ICU where the study was conducted ET fixation of the patients in the study group was performed with an ET holder AnchorFast Oral Endotracheal Tube Fastener Hollister Liberlyville USA when they arrived at the CVS ICU

When the findings of patients suction needs were observed increase in respiratory rate HR increase arterial BP increase high pressure alarm in ventilator mucus in ET cyanosis dyspnea restlessness sweating disturbance of blood gas parameters wheezing etc endotracheal suction was performed according to the application standards The patients SBP DBP HR and SpO2 values which were displayed on the bedside monitor Nihon Kohden Tokyo were recorded on the Hemodynamic Parameters Form just before during and at the end of endotracheal suction and in the following 5th and 15th minutes

During the suction process it was ensured that the patients were in the supine position in which the head of the bed was lifted by 30 degree Before the intra-arterial BP was measured the transducer was reset at the level of the right atrial plebostatic axis and the position was not changed during all the measurements

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None