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Investigation of the applicability of dry powder inhalation in school children

Investigation of the applicability of dry powder inhalation in school children - Dry powder inhalation in school children

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37634
Enrollment
80
Registered
2012-06-06
Start date
2012-06-25
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cystic fibrosis mucoviscidosis

Interventions

None listed

Sponsors

Rijksuniversiteit Groningen
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: • Registered at the primary school • Informed consent of parent(s)/guardian(s) • Assent of the child

Exclusion criteria

Exclusion criteria: No exclusion criteria are formulated. In principle, all children registered at the primary school are eligible to participate.

Design outcomes

Primary

MeasureTime frame
The main study parameter is the ability of a child to understand how to use the inhaler correctly.

Secondary

MeasureTime frame
The parameter that describes whether or not a child is capable of using the inhaler correctly is the pressure drop (s)he creates over the inhaler upon inhalation, from which various inspiratory parameters can be calculated. Furthermore, the presence of a blockage in the mouth upon inhalation will be observed as function of the inhaler design (mouthpiece and resistance).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)