Pain, Acute Clinical Trial
Official title:
iCAP Mini - The Influence of Skin-to-skin Contact on Cortical Activity During Painful Procedures on Preterm Infants in the Neonatal Intensive Care Unit: A Randomized Control Trial
The aim of this study is to examine the effect of SSC compared to sucrose on pain induced activity in the preterm infant brain using: a) series of low intensity experimental stimuli (PinPrick);and b) medically required heel lance. Secondary objectives include determining: a) differences between behavioral pain response and pain response during heel lance; and b) rate of adverse events across groups.
Hospitalized preterm infants undergo an average of 12 painful procedures daily, with less
than half receiving pain relief. Poorly treated early pain can have long lasting negative
effects that impact later learning, development, and reaction to future pain, stress, and
emotional experiences. While sweet tasting solution (sucrose) is considered the standard of
care for reducing behavioral responses to acute procedural pain in preterm infants, some
evidence that sucrose may not similarly reduce pain related brain activity raises concerns
regarding the degree of pain relieving effect. This concern is especially relevant as the use
of sucrose to manage repeated acute pain has not been found to prevent heightened later pain
associated with this exposure. Strong evidence suggests that maternal infant skin-to-skin
contact (SSC) is effective in reducing behavioral responses to pain. Given the multi-sensory
benefits of SSC, it is highly likely that SSC provided during pain in early life may reduce
pain induced brain activity.
Infants ( n=126) (32 to 36 completed weeks gestational age) admitted to the Neonatal
Intensive Care Unit, and their mothers within the first seven days of age will be randomly
assigned to receive: i) SSC or ii) 24 % oral sucrose. Each baby will receive both the
PinPrick and heel lance, following a no treatment baseline period. The primary outcome is
pain related brain activity measured using an electroencephalogram (EEG) pain-specific
event-related potential. Secondary outcomes include pain intensity measured using a
behavioural infant pain assessment tool (Premature Infant Pain Profile-Revised) and rate of
adverse events.
This will be the first study to examine the effect of SSC on pain induced brain activity in
the preterm infant brain during experimental and clinical pain stimuli, measured using EEG.
Given the negative neurodevelopmental outcomes associated with unmanaged pain, it is
imperative that preterm infants receive the most effective pain relieving treatments to
improve their health outcomes.
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