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Measuring the doserespons of Salbutamol (Ventolin) by means of a lungfunctiontest

Measuring the doserespons of Salbutamol (Ventolin) by means of a lungfunctiontest - Do-Re-Mi-study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47492
Enrollment
170
Registered
2017-06-01
Start date
2017-09-18
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

n.v.t.

Interventions

None listed

Sponsors

HagaZiekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: n.v.t.

Exclusion criteria

Exclusion criteria: n.v.t.

Design outcomes

Primary

MeasureTime frame
n.v.t.

Secondary

MeasureTime frame
n.v.t.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)