Asthma Trial, Recruiting NCT06902766 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Asthma
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Asthma Trial, Recruiting

NCT06902766
Recruiting Not Applicable

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:

  • Your child is between 4 and 12 years old and has been diagnosed with asthma by a doctor.
  • Your child is already being seen regularly for their asthma by a paediatrician or lung specialist for children.
  • Your child's asthma falls into a moderate or more serious category, according to international asthma guidelines (GINA grades 2, 3, or 4 — confirm with trial site if unsure which grade applies to your child).
  • Your child uses pressurised inhaler devices (the standard type of inhaler that releases a puff of medicine) for both their regular and relief asthma medicines.
  • Your child is covered by social security (French health insurance).
  • A parent or legal guardian has agreed in writing to take part in the study alongside their child.
  • There is a compatible smartphone available in the household that can download the study app.
  • The parent or guardian is able, in the investigator's opinion, to understand how to use the study app and the special digital inhalers provided.

Who may not be able to join:

  • Children who have another health condition that could affect the study results, such as certain lung conditions like bronchopulmonary dysplasia or cystic fibrosis (confirm with trial site for other conditions).
  • Children whose parent or legal guardian is not able, in the investigator's opinion, to understand the purpose of the study or to give their consent.
  • Children who receive State Medical Aid (Aide Médicale d'État) as their health coverage.
  • Children who did not use the study inhaler system within 15 days of joining the trial.

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 22 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: David DUMMOND, MD, PhD, Hôpital Necker Enfants Malades AP-HP

Phone: 01 87 89 20 28

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
25 November 2025
Est. completion
1 January 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Change in asthma severity measured by the Composite Asthma Severity Index (CASI)

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: 22 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