The Effect of Surgical Incision Drep Use in Endotracheal Tube Fixation
ConditionPreterm
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age28-34
SponsorHasan Kalyoncu University
About this trial
It is aimed to minimise both unplanned extubation and skin damage with the surgical incision drep that we will use to fix the endotracheal tube in neonatal preterm infants and to reduce the complications that may develop due to these events. In addition, it is aimed to evaluate the relationship between these parameters by using devices measuring skin moisture, skin pH and Neonatal Skin Condition Assessment Scale in experimental and control groups.
Eligibility criteria
Qualifiers
Preterm infants between 28-34 weeks of gestation hospitalized in neonatal intensive care unit,
Intubated infants on invasive mechanical ventilators,
Babies who were orally intubated were included in the study.
Disqualifiers
Congenital skin condition,
With circulatory problems,
Congenital anomalies and metabolic disorders,
Small for gestational age (SGA) and large for gestational age (LGA),
Trial design
Treatments tested in this trial
- surgical incision drep
Treatment groups
110 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov