Phase 3 Asthma Trial, Recruiting NCT06785272 Sponsor: Suzanne Schuh Condition: Asthma
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Phase 3 Asthma Trial, Recruiting

NCT06785272
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Children aged between 2 and 17 years old (before their 18th birthday).
  • Children who have been diagnosed with asthma or an asthma-like condition by a doctor, including an emergency department doctor.
  • Children whose asthma is considered moderate to severe after already receiving three rounds of inhaled breathing treatments (salbutamol and ipratropium) in the emergency department, based on a specific symptom score of 5 or higher.

Who may not be able to join:

  • Children who have already received intravenous magnesium (a medication given through a drip) within the 24 hours before arriving at the emergency department.
  • Children who need immediate breathing support on arrival, such as a special high-flow oxygen mask, a breathing machine, or a breathing tube inserted into the airway. (Note: basic supplemental oxygen on its own does not disqualify a child.)
  • Children known to have kidney disease, a long-term lung condition, a neurological condition, a heart condition, or another serious ongoing illness.
  • Children with a known allergy or sensitivity to magnesium sulfate.
  • Children who have previously taken part in this trial.
  • Families where neither English nor French is understood well enough to give informed consent.
  • Families without access to a phone or email, or who would be otherwise unavailable for follow-up contact after the visit.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Suzanne Schuh, MD, The Hospital for Sick Children

Phone: 416-813-7654

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Suzanne Schuh
Registry
ClinicalTrials.gov
Start date
8 October 2025
Est. completion
1 October 2027

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Pediatric Respiratory Assessment Measure (PRAM) score: This score ranges from 0-12. A score from 0-3 is mild, 4-7 moderate and 8-12 severe. A low score is a better outcome and a high score is a worse outcome.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov