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The pharmacokinetics of intravenous salbutamol in pediatric status asthmaticus: a pilot study.

The pharmacokinetics of intravenous salbutamol in pediatric status asthmaticus: a pilot study. - The pharmacokinetics of intravenous salbutamol.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37955
Enrollment
20
Registered
2010-12-14
Start date
2011-09-15
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

acute severe asthma status asthmaticus

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Age 0 to 18 years-admitted to the hospital because of status asthmaticus- Need for continuous salbutamol nebulisation (more than 3 times/ hour)- Patient/parental informed consent

Exclusion criteria

Exclusion criteria: - Withdrawal of informed consent

Design outcomes

Primary

MeasureTime frame
The main study parameter is the description of the pharmacokinetic parameters of intravenous salbutamol.

Secondary

MeasureTime frame
Secondary study parameters are the efficacy (asthma scores) and safety (occurrence of side-effects) of intravenous salbutamol.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)