What helps choking in babies under age two: a look at real-life interventions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort study collects data on out-of-hospital choking events involving children aged 2 years or younger in Alberta. It documents the interventions performed by bystanders or healthcare providers and tracks subsequent EMS assessment or emergency department care. The goal is to compare different techniques used during FBAO incidents to identify approaches associated with better outcomes and lower risk. Data are gathered from real-world emergency responses and hospital encounters rather than a controlled trial. The lead sponsor is the University of Calgary, with data collection occurring virtually within Calgary, Alberta.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* \- Young children (aged 2 years or less) who experienced an out-of-hospital FBAO in Alberta, Canada
* Received a FBAO intervention by bystander or healthcare provider
* Were assessed by EMS at the time of the incident, or later attended an emergency department due to the incident

Exclusion Criteria:

\- Patients with abnormal airway anatomy such as a tracheostomy.

Where it's running

• Virtual
  Calgary, Alberta, Canada Recruiting

Study contacts

• Principal investigator: Cody Dunne, MD — University of Calgary
• Study coordinator: Cody Dunne
• Email: cody.dunne@ucalgary.ca
• Phone: 000-000-0000

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Choking interventions in adults and children: what works when someone is blocking the airway

  This study observes real-world choking events in Alberta to see which bystander or EMS treatments help people who are over 2 years old.

  Recruiting University of Calgary · Calgary, Alberta · NCT07814690

• Cerebral oximetry-guided care after cardiac arrest

  This study tests whether using a brain oxygen monitor can help guide treatment for adults who have had a cardiac arrest to protect the brain and improve outcomes.

  Recruiting University of Calgary · Calgary, Alberta · NCT07829887

• Understanding growth hormone deficiency after a brain injury in adults

  This observational study tests whether growth hormone deficiency affects quality of life and symptoms in adults with traumatic brain injury and whether GH replacement helps after 12 weeks.

  Recruiting University of Calgary · Calgary, Alberta and 1 other locations · NCT07795736

• Intra-arterial Thrombolysis After Endovascular Thrombectomy in AIS

  This trial tests whether giving intra-arterial thrombolysis with tenecteplase or alteplase after endovascular thrombectomy helps improve recovery in adults with acute ischemic stroke.

  Recruiting Phase 3 University of Calgary · Sydney, Barangaroo and 12 other locations · NCT07687056

• Impact of a Clinical Information System on hospital outcomes for adults with chronic diseases

  This study tests whether implementing a Clinical Information System helps reduce readmissions or death within 30 days after hospital discharge for adults with chronic conditions in Alberta.

  Recruiting University of Calgary · Calgary, Alberta · NCT07609381

• Health, Equity, and Resilience in Girls and Women with ADHD Across the Lifespan

  This study tests health and well-being measures in girls and women with and without ADHD across Canada to see how ADHD relates to life phases and experiences.

  Recruiting University of Calgary · Calgary, Alberta · NCT07597707

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.