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Comparison Three Methods on Endotracheal Aspiration in Preterm Infants

NCT05434364 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2024-10-15

No results posted yet for this study

Summary

Stress and pain control are vital for newborns, especially preterm babies. While painful procedures cause physiological changes in the short term, they negatively affect brain development in the long term. Non-pharmacological interventions with proven efficacy include: fetal position, sucrose, breastfeeding, breast milk, maternal presence, non-nutritive sucking, swaddling (wrapping) and skin-to-skin contact, as well as developmentally supportive positioning. Evaluating the effectiveness of nursing practices to be performed on babies, scientifically proving the most beneficial application that will both alleviate pain and increase their comfort in painful procedures such as aspiration and being more beneficial to babies are among the most basic benefits. Thanks to these applications, it is predicted that your baby will experience less pain and provide more comfort. Therefore, this study aim to comparison the effects of facilitated tucking, swaddling and prone position applied during endotracheal aspiration on pain, comfort and physiological parameters in preterm infants.

Conditions

  • Preterm
  • Pain, Acute
  • Physiological Stress
  • Nursing Care
  • Comfort

Interventions

OTHER

Facilitated Tucking

giving facilitated tucking before (1st and 3th minutes), during and after (1st and 3th minutes) the procedure

OTHER

Swaddling

swaddling before (1st and 3th minutes), during and after (1st and 3th minutes) the procedure

OTHER

Prone Position

giving prone position before (1st and 3th minutes), during and after (1st and 3th minutes) the procedure

Sponsors & Collaborators

  • Kilis 7 Aralik University

    collaborator OTHER

  • Istanbul University - Cerrahpasa

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
28 Weeks
Max Age
35 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-03
Primary Completion
2024-07-03
Completion
2024-09-03

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05434364 on ClinicalTrials.gov