ClinConnect ClinConnect Logo
Search / Trial NCT07000877

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

Launched by TELETHON KIDS INSTITUTE · May 22, 2025

Trial Information

Current as of July 01, 2025

Not yet recruiting

Keywords

Perioperative Respiratory Adverse Events Nasal Decongestant Upper Respiratory Tract Infection Children Surgery Pediatrics Anesthesia

ClinConnect Summary

This clinical trial is designed to see if a nasal spray can help children who have a cold or upper respiratory infection breathe better during and after surgery. The researchers want to find out if using this nasal spray, which helps open up the nasal passages, can reduce breathing problems that might happen when children wake up from anesthesia or in the recovery area afterward. They will compare the nasal spray to a placebo, which looks the same but doesn’t contain any medicine, to see if it really makes a difference.

To participate in this study, children aged 1 to nearly 9 years old who have had a cold or infection in the last two weeks and are scheduled for surgery with general anesthesia may be eligible. Participants will take either the nasal spray or the placebo just before their surgery and will be closely monitored during and after the procedure for any breathing issues. Parents and children will also be asked how they felt about using the nasal spray. This study is not yet recruiting, but it aims to help improve the safety and comfort of children undergoing surgery.

Gender

ALL

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) or receiving co-phenylocaine or decongestion for surgery.
  • Surgery impacting the nasal airflow, e.g. adenoidectomy, cautery of inferior turbinates.
  • Airway management with an endotracheal tube, face mask or high flow nasal oxygen.
  • Known cardiovascular, respiratory or neurological disorders giving an ASA III or above.
  • Thyroid disease.
  • Diabetes.
  • Known hypersensitivity to the interventional products.
  • Department of Child Protection and Family Services involved in their care.
  • Planned admissions to the Paediatric Intensive Care Unit (PICU).

About Telethon Kids Institute

The Telethon Kids Institute is a leading Australian research organization dedicated to improving the health and well-being of children through innovative and impactful research. Committed to translating scientific discoveries into practical applications, the Institute focuses on a wide range of pediatric health issues, including developmental disorders, infectious diseases, and chronic conditions. By fostering collaboration between researchers, clinicians, and the community, the Telethon Kids Institute aims to drive advancements in child health and promote evidence-based practices that enhance the quality of life for children and their families. Through its rigorous clinical trials and commitment to ethical research practices, the Institute plays a crucial role in shaping the future of pediatric healthcare.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported