Aprepitant Treatment to Prevent Postoperative Nausea and Vomiting in Children Undergoing Scoliosis Surgery

Recruiting Phase 2 Interventional Study
Spinal Fusion Nausea and Vomiting, Postoperative Anesthesia
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
8 – 19
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Prevention
Participants needed
100 (estimated)
Sponsor
IWK Health Centre · Other
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About This Trial

This research trial will measure how useful Aprepitant is in preventing nausea and vomiting in children having surgery to correct scoliosis (curvature of the spine).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Posterior Spinal Instrumentation and Fusion (PSIF) for idiopathic scoliosis * The fusion must include at least 6 vertebral levels. * Children greater than or equal to 8 years old, and less than 19 years old on the day of surgery * Weight \> 40kg - for ease of pharmacy preparat…
Contacts

Mathew Kiberd, MD

7789841329

mathew.kiberd@iwk.nshealth.ca

CONTACT

Tristain Dumbarton, MD

9022401356

tristan.dumbarton@iwk.nshealth.ca

CONTACT