Palonosetron
Drugpalonosetron IV 1 mcg/kg
NCT Number: NCT00828295
The objective of the study is to assess the safety and efficacy of two doses of IV palonosetron each administered as a single dose for the prevention of postoperative nausea and vomiting through 72 hours postoperatively in children aged 28 days up to 16 years inclusive undergoing surgical procedures requiring general endotracheal inhalation anesthesia.
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Notify Me28 day–16 year
All sexes
Interventional
Phase 3
Federal State Institution Central Research Institute of Traumatology and Orthopedics n.a. N.N. Priorov under the Federal Agency for High-Tech Medical Care, Moscow, Russia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
MAIN INCLUSION CRITERIA
MAIN EXCLUSION CRITERIA
palonosetron IV 1 mcg/kg
Time frame: 0-72 hours post-operatively
Time frame: 0-24 hours
Complete Response defined as no vomiting, no retching, and no use of rescue medication
Helsinn Healthcare SA
Industry
A Multicenter, Double-blind, Randomized, Parallel Group, Stratified Study to Assess the Safety and Efficacy of Single IV Doses of Palonosetron to Prevent Postoperative Nausea and Vomiting in Pediatric Patients
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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