Status:
UNKNOWN
Pain Perception Associated With Orogastric Tube Insertion in Preterm Infants
Lead Sponsor:
Afyonkarahisar Health Sciences University
Conditions:
Orogastric Tube Insertion
Eligibility:
All Genders
Phase:
NA
Brief Summary
This study is a randomized controlled experimental study designed to examine the effect of white noise and swaddling methods in reducing the pain caused by orogastric tube insertion in preterm infants...
Detailed Description
This is a randomized controlled experimental study designed to examine the effect of white noise and swaddling methods in reducing the pain caused by orogastric tube insertion in preterm infants. The...
Eligibility Criteria
Inclusion
- With 32-34 weeks of gestation,
- With the postnatal age between 3-28 days,
- Birth weight is above 1000 grams,
- With the Apgar score ≥7 at 1st and 5th minutes,
- With stable vital signs,
- Without any congenital anomaly,
- Not receiving mechanical ventilator support and having spontaneous breathing,
- Requested by the physician to place an orogastric tube and fed with an orogastric tube,
- Breastfeeding (through an orogastric tube),
- Not experienced a painful procedure at least half an hour before the interventions,
- Without the use of opioid or non-opioid analgesic in their treatment,
- Without congenital or acquired malformation related to hearing,
- With parents written consent for the participation of their baby.
Exclusion
- With the postnatal age outside 3-28 days,
- Birth weight is ≤ 1000 grams,
- With the Apgar score \<7 at 1st and 5th minutes,
- With unstable vital signs,
- With congenital anomaly in the face or the oral cavity,
- Being on mechanical ventilator support,
- With a congenital malformation that may affect respiration and cause asphyxia,
- With intracranial bleeding or risk of bleeding,
- With disorders affecting the cerebral circulation or cardiovascular system,
- Subjected to a painful procedure at least half an hour before the interventions,
- With opioid or non-opioid analgesic in their treatment,
- With the surgical history,
- With continuous sedative treatment,
- With congenital or acquired malformation related to hearing,
- Not being fed with an orogastric tube,
- With parent not giving consent for the participation of their baby
Key Trial Info
Start Date :
January 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 15 2022
Estimated Enrollment :
132 Patients enrolled
Trial Details
Trial ID
NCT04678570
Start Date
January 1 2021
End Date
October 15 2022
Last Update
July 21 2022
Active Locations (1)
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1
Uşak Öztan Hospital Neonatal Intensive Care Unit
Uşak, Turkey (Türkiye)