ClinicalTrials.Veeva

Menu

Facilitated Tucking Position During Endotracheal Suctioning

K

Kafrelsheikh University

Status

Completed

Conditions

Respiratory Distress Syndrome

Treatments

Procedure: tucking position during endotracheal suctioning

Study type

Interventional

Funder types

Other

Identifiers

NCT06428916
KafrelsheikhU2

Details and patient eligibility

About

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.

Enrollment

40 patients

Sex

All

Ages

32 to 36 weeks old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Study Group
Experimental group
Description:
Consisted of 20 neonates who will receive tucking position during endotracheal suctioning
Treatment:
Procedure: tucking position during endotracheal suctioning
Control group
No Intervention group
Description:
Consisted of 20 neonates who will receive routine care during Endotracheal suctioning

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems