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Clinical Trials/NCT06428916
NCT06428916
Completed
Not Applicable

The Effect of Facilitated Tucking Position During Endotracheal Suctioning on Physiological Measurement and Behavioral Responses of the Preterm Neonates

Kafrelsheikh University1 site in 1 country40 target enrollmentDecember 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Distress Syndrome
Sponsor
Kafrelsheikh University
Enrollment
40
Locations
1
Primary Endpoint
Change from baseline of Respiratory Rate of preterm neonates on Neonates' Physiological Assessment Tool during and immediately following the endotracheal suction procedure
Status
Completed
Last Updated
last year

Overview

Brief Summary

Aim of the present study The present study will aimed to determine the effect of facilitated tucking position during endotracheal suctioning on physiological criteria and behavioural responses of the preterm neonates.

Research Hypotheses

  1. Preterm neonates who receive facilitated tucking position during endotracheal suctioning exhibit more stable physiological criteria than those who do not.
  2. Preterm neonates who receive facilitated tucking position during endotracheal suctioning exhibit more stable behavioral responses than those who do not.
Registry
clinicaltrials.gov
Start Date
December 1, 2022
End Date
July 30, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Eman Wardany Abdelaal Mohamed

assistant professor of pediatric nursing

Kafrelsheikh University

Eligibility Criteria

Inclusion Criteria

  • Gestational age between 32 and 36 weeks, weight 1200 grams or greater.
  • Postnatal age: two days after delivery to allow for resolution of analgesia or anesthesia received by their mothers during labor.
  • Have endotracheal intubation.

Exclusion Criteria

  • Preterm neonates who have congenital anomalies or neurological malformations, intracranial hemorrhage, seizures.
  • Preterm neonates who received sedatives within four hours before the intervention
  • Preterm neonates who exposed to any uncomfortable procedure for at least 30 minutes prior to the intervention.

Outcomes

Primary Outcomes

Change from baseline of Respiratory Rate of preterm neonates on Neonates' Physiological Assessment Tool during and immediately following the endotracheal suction procedure

Time Frame: during procedural and immediately after procedure

Neonates' Physiological Assessment Tool was developed by researchers after a review of relevant literature to assess Physiological Parameters of preterm neonates as Respiratory Rate (RR)

Change from baseline of oxygen saturation in blood of preterm neonates on Neonates' Physiological Assessment Tool during and immediately following the endotracheal suction procedure

Time Frame: during procedural and immediately after procedure

Neonates' Physiological Assessment Tool was developed by researchers after a review of relevant literature to assess Physiological Parameters of preterm neonates as oxygen saturation in blood(SPO2)

Change from baseline of heart rate of preterm neonates on Neonates' Physiological Assessment Tool during and immediately following the endotracheal suction procedure

Time Frame: during procedural and immediately after procedure

Neonates' Physiological Assessment Tool was developed by researchers after a review of relevant literature to assess Physiological Parameters of preterm neonates as Heart Rate (HR)

Secondary Outcomes

  • change of baseline of Neonates' behavioral states on Anderson Behavioral State Scale during and immediately following the endotracheal suction procedure(during procedural and immediately after procedure)

Study Sites (1)

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