Pain Clinical Trial
Official title:
Intranasal Hydromorphone for the Treatment of Acute Pain in Children: A Pilot Study.
Intranasal hydromorphone has been shown to be effective in reducing acute pain in adults. It
has not been previously studied in children, but may be a viable option for effectively and
safely reducing pain in children by administering an analgesic by the intranasal route.
This study will be a prospective, open-label pilot study of intranasal hydromorphone in
children with moderate to severe acute pain presenting to the pediatric emergency department.
The investigators aim to describe the amount of pain reduction associated with intranasal
hydromorphone, and to determine the optimal dose of intranasal hydromorphone associated with
a clinically meaningful improvement in acute pain.
Primary Aim: Determine the change in pain intensity in children with moderate to severe pain
who receive intranasal hydromorphone one hour after administration.
Secondary Aim(s): Describe the incidence of minor and major adverse events associated with
intranasal hydromorphone in children with acute pain.
The investigators will assess the patient's pain at baseline (prior to study drug
administration), then after study drug administration: 5 minutes, 15 minutes, 30 minutes, 45
minutes, 60 minutes, and then every 30 minutes thereafter until 6 hours; administration of
non-protocolized rescue medication administration (i.e. administered after first two rescue
doses of IN hydromorphone); or discharge from emergency department (whichever comes first).
The pain score at 60 minutes will be the primary outcome.
The investigators will evaluate qualitative improvement in pain intensity at 15- and
30-minutes after study drug administration. If there is no improvement, or worsening of pain
intensity, at each assessment, an additional rescue dose rescue dose of intranasal
hydromorphone will be administered. After 60 minutes, the treating physician may administer
any additional rescue medications at their discretion to treat the child's pain.
The patient will be assessed for minor and major adverse events for the duration of the
study.
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