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The Effect of the Position Given to the Child After Weaning from Noninvasive Mechanical Ventilation on Physiological Symptoms

NCT ID: NCT06580522

Last Updated: 2024-08-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-01

Study Completion Date

2024-07-26

Brief Summary

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The aim of this clinical trial was to investigate the effect of the position given to children after weaning from noninvasive mechanical ventilation on the physiological symptoms (heart rate, oxygen saturation, respiratory rate and blood pressure) of children aged six months to six years in the Pediatric Intensive Care Unit.

Detailed Description

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Conditions

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Prone Position Supine Position Child

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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Prone Position Group

Children in this group were given the prone position after weaning from noninvasive mechanical ventilation and its effect on the physiologic symptoms of the children was examined.

Group Type EXPERIMENTAL

Prone Position Group

Intervention Type OTHER

After the children in the prone position group were weaned from noninvasive mechanical ventilation according and started to breathe spontaneously, they were prone positioned and monitored for 120 minutes (2 hours) every 20 minutes (0.min, 20.min, 40.min, 60.min, 80.min, 100.min, 120.min) with a head-monitor for peak heart rate, oxygen saturation, respiratory rate and blood pressure.

Supine Position Group

Supine position group children were given supine position after weaning from noninvasive mechanical ventilation and the effects on physiologic symptoms were examined.

Group Type EXPERIMENTAL

Supine Position Group

Intervention Type OTHER

After the children in the supine position group were weaned from noninvasive mechanical ventilation according and started to breathe spontaneously, they were supine positioned and monitored for 120 minutes (2 hours) every 20 minutes (0.min, 20.min, 40.min, 60.min, 80.min, 100.min, 120.min) with a head-monitor for peak heart rate, oxygen saturation, respiratory rate and blood pressure.

Interventions

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Prone Position Group

After the children in the prone position group were weaned from noninvasive mechanical ventilation according and started to breathe spontaneously, they were prone positioned and monitored for 120 minutes (2 hours) every 20 minutes (0.min, 20.min, 40.min, 60.min, 80.min, 100.min, 120.min) with a head-monitor for peak heart rate, oxygen saturation, respiratory rate and blood pressure.

Intervention Type OTHER

Supine Position Group

After the children in the supine position group were weaned from noninvasive mechanical ventilation according and started to breathe spontaneously, they were supine positioned and monitored for 120 minutes (2 hours) every 20 minutes (0.min, 20.min, 40.min, 60.min, 80.min, 100.min, 120.min) with a head-monitor for peak heart rate, oxygen saturation, respiratory rate and blood pressure.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Between 6 months and 6 years of age
* Being monitored for respiratory diseases
* Weaning from noninvasive mechanical ventilation during the research process
* Body temperature within the normal range (36 centigrade-37,5 centigrade)
* Verbal and written consent to participate in the study given by their parents

Exclusion Criteria

* Congenital anomaly
* Surgical intervention that prevents supine/prone positioning
* Development of pneumothorax during research
* Hypoxia during the research
Minimum Eligible Age

6 Months

Maximum Eligible Age

6 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role collaborator

Acibadem University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Duygu Gözen, Prof.Dr.

Role: STUDY_DIRECTOR

Koç Üniversitesi

Locations

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Istanbul University Cerrahpasa Medical Faculty Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2023/30

Identifier Type: -

Identifier Source: org_study_id