Nasal Decongestant to Reduce Perioperative Adverse Events in Children With Upper Respiratory Track Infections Having Anesthesia.

Recruiting Phase 4 Interventional Study
Perioperative Respiratory Adverse Events Anesthesia Outcomes
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
1 – 8
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Prevention
Participants needed
200 (estimated)
Sponsor
Telethon Kids Institute · Other
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About This Trial
The goal of this multicentre, double-blind, randomised controlled trial study is to learn if the use of a nasal spray to open the nasal passages and increase airflow before surgery can reduce the occurrence of perioperative respiratory adverse events in children with upper respiratory tract infection who are undergoing anesthesia. The main questions it aims to answer are: * Does use of a nasal d…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Children aged 1 to 8.99 years with a current or recent upper respiratory tract infection (\<2 weeks). * Undergoing interventions or surgery under general anesthesia (elective or urgent not emergency). Exclusion Criteria: * Currently taking nasal decongestants (past 24 hours)…
Contacts

Britta S. von Ungern-Sternberg, MD PHD

+618 6456 4806

britta.regli-vonungern@health.wa.gov.au

CONTACT